A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970657



Internal ID18605879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32642773..32655318hg38UCSC Ensembl
Innerchr6:32610550..32623095hg19UCSC Ensembl
Innerchr6:32718528..32731073hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3812546
hg1912546
hg1812546
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2761094, nssv2764246, nssv2761437, nssv2757335, nssv2766285, nssv2765606
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00542, HGDP00456
Known GenesHLA-DQA1
MethodSequencing
AnalysisChimpanzee CNVs
Human CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970657
Frequency
Sample Size10
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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