A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637701



Internal ID7024491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4719936..4722366hg38UCSC Ensembl
Innerchr16:4719936..4722366hg38UCSC Ensembl
Outerchr16:4719561..4722701hg38UCSC Ensembl
chr16:4769937..4772367hg19UCSC Ensembl
Innerchr16:4769937..4772367hg19UCSC Ensembl
Outerchr16:4769562..4772702hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg382431
hg192431
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15363792, essv15363749, essv15363731, essv15363799, essv15363774, essv15363772, essv15363761, essv15363747, essv15363773, essv15363740, essv15363754, essv15363758, essv15363784, essv15363755, essv15363770, essv15363776, essv15363760, essv15363790, essv15363767, essv15363787, essv15363763, essv15363752, essv15363765, essv15363782, essv15363768, essv15363785, essv15363732, essv15363756, essv15363751, essv15363777, essv15363733, essv15363753, essv15363735, essv15363786, essv15363746, essv15363793, essv15363779, essv15363739, essv15363798, essv15363788, essv15363795, essv15363769, essv15363775, essv15363762, essv15363745, essv15363759, essv15363783, essv15363797, essv15363738, essv15363748, essv15363741, essv15363781, essv15363743, essv15363730, essv15363780, essv15363750, essv15363744, essv15363789, essv15363766, essv15363771, essv15363796, essv15363742, essv15363757, essv15363729, essv15363778, essv15363791, essv15363764, essv15363737, essv15363736, essv15363794, essv15363734
SamplesNA20891, NA19794, HG00361, NA18980, NA20864, HG00179, HG00177, NA19443, HG00109, HG00122, HG01702, NA20756, HG00330, NA19054, HG03629, HG00369, NA12761, NA12282, HG02143, HG00106, HG01495, HG03693, HG01525, HG01133, HG00178, NA20533, NA20818, NA11831, HG00313, HG00154, HG01435, NA20524, HG02697, HG01790, HG03919, HG01447, HG01073, HG01414, HG02787, HG03953, HG03238, HG00258, HG04025, HG03848, HG00119, HG00285, NA19749, HG02220, NA19732, HG01685, HG00136, HG00638, HG01977, HG01108, NA19783, NA06986, HG01991, NA21125, HG01785, NA20849, NA12749, HG03863, HG01055, HG03022, NA20510, HG00274, HG00105, NA07056, NA19758, HG01926, HG03741
Known GenesANKS3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637701
Frequency
Sample Size2504
Observed Gain0
Observed Loss71
Observed Complex0
Frequencyn/a


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