A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694232



Internal ID15430884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:5777313..5787167hg38UCSC Ensembl
Innerchr6:5777546..5787400hg19UCSC Ensembl
Innerchr6:5722545..5732399hg18UCSC Ensembl
Innerchr6:5722545..5732399hg17UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg389855
hg199855
hg189855
hg179855
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518398
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694232
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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