A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697221



Internal ID15433873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:163171222..163176071hg38UCSC Ensembl
Innerchr6:163592254..163597103hg19UCSC Ensembl
Innerchr6:163512244..163517093hg18UCSC Ensembl
Innerchr6:163562665..163567514hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg384850
hg194850
hg184850
hg174850
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520096
Supporting Variants
Samples
Known GenesPACRG
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697221
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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