A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv664618



Internal ID15054584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:24705607..24709602hg38UCSC Ensembl
Innerchr6:24705835..24709830hg19UCSC Ensembl
Innerchr6:24813814..24817809hg18UCSC Ensembl
Innerchr6:24813814..24817809hg17UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg383996
hg193996
hg183996
hg173996
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515732
Supporting Variants
Samples
Known GenesC6orf62
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv664618
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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