A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2765606



Internal ID17762336
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 Number1
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv970657
Supporting Variants
SamplesHGDP00542
Known GenesHLA-DQA1
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2765606
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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