A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701767



Internal ID15438419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:9590543..9765660hg38UCSC Ensembl
Innerchr6:9590776..9765893hg19UCSC Ensembl
Innerchr6:9698762..9873879hg18UCSC Ensembl
Innerchr6:9698762..9873879hg17UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38175118
hg19175118
hg18175118
hg17175118
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525621
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701767
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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