A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637779



Internal ID6677880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:6907701..6908487hg38UCSC Ensembl
Innerchr16:6907701..6908487hg38UCSC Ensembl
Outerchr16:6907377..6908757hg38UCSC Ensembl
chr16:6957702..6958488hg19UCSC Ensembl
Innerchr16:6957702..6958488hg19UCSC Ensembl
Outerchr16:6957378..6958758hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38787
hg19787
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15365790, essv15365796, essv15365746, essv15365783, essv15365760, essv15365792, essv15365770, essv15365767, essv15365763, essv15365778, essv15365789, essv15365755, essv15365742, essv15365762, essv15365786, essv15365781, essv15365787, essv15365800, essv15365777, essv15365788, essv15365772, essv15365748, essv15365745, essv15365780, essv15365759, essv15365791, essv15365757, essv15365776, essv15365764, essv15365771, essv15365752, essv15365799, essv15365749, essv15365774, essv15365775, essv15365798, essv15365761, essv15365773, essv15365768, essv15365793, essv15365750, essv15365766, essv15365754, essv15365779, essv15365784, essv15365743, essv15365758, essv15365753, essv15365769, essv15365765, essv15365747, essv15365744, essv15365797, essv15365782, essv15365801, essv15365785, essv15365794, essv15365751, essv15365756, essv15365795
SamplesHG00096, NA12717, HG00121, HG01773, NA19914, HG01079, NA20752, HG00103, HG00097, NA12155, NA12413, HG00138, HG01682, HG00122, HG00129, NA12348, HG00346, HG01354, HG01063, HG01365, NA20541, NA12282, HG00120, HG00106, HG02224, NA20812, HG00113, NA12815, NA20811, HG00160, HG00338, HG00159, HG01771, NA12748, NA11831, HG00313, NA20535, HG01248, NA19707, NA12872, HG01790, HG01789, NA20809, HG00101, HG00132, NA20581, NA06989, HG00321, HG00140, HG01334, HG00146, NA19756, HG00099, NA12778, HG00336, NA20792, NA06986, NA21090, HG01468, NA21104
Known GenesRBFOX1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637779
Frequency
Sample Size2504
Observed Gain0
Observed Loss60
Observed Complex0
Frequencyn/a


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