A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657957



Internal ID15047923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31393708..31491965hg38UCSC Ensembl
Innerchr6:31361485..31459742hg19UCSC Ensembl
Innerchr6:31469464..31567721hg18UCSC Ensembl
Innerchr6:31469464..31567721hg17UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3898258
hg1998258
hg1898258
hg1798258
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517441
Supporting Variants
Samples
Known GenesHCG26, HCP5, MICA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657957
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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