A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620011



Internal ID7006884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:23290061..23299939hg38UCSC Ensembl
Innerchr9:23290061..23299939hg38UCSC Ensembl
Outerchr9:23289738..23300188hg38UCSC Ensembl
chr9:23290059..23299937hg19UCSC Ensembl
Innerchr9:23290059..23299937hg19UCSC Ensembl
Outerchr9:23289736..23300186hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg389879
hg199879
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13428624, essv13428618, essv13428610, essv13428614, essv13428599, essv13428623, essv13428620, essv13428609, essv13428611, essv13428617, essv13428608, essv13428627, essv13428625, essv13428626, essv13428621, essv13428598, essv13428612, essv13428604, essv13428601, essv13428615, essv13428600, essv13428606, essv13428619, essv13428605, essv13428597, essv13428630, essv13428631, essv13428602, essv13428607, essv13428622, essv13428628, essv13428629, essv13428603, essv13428616, essv13428613
SamplesNA18592, NA18599, HG01806, NA19067, NA19076, NA19728, NA19649, NA19088, NA19782, NA18749, HG01550, NA19789, HG02134, NA18605, NA19056, HG01271, NA20314, NA19788, NA19658, NA19064, NA19655, NA19740, HG02286, NA18950, HG00638, HG01396, NA19741, NA19083, HG02410, NA19726, HG02182, HG01872, NA19661, NA19758, NA18612
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620011
Frequency
Sample Size2504
Observed Gain0
Observed Loss35
Observed Complex0
Frequencyn/a


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