A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700673



Internal ID15090639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:94286803..94402933hg38UCSC Ensembl
Innerchr6:94996521..95112651hg19UCSC Ensembl
Innerchr6:95053242..95169372hg18UCSC Ensembl
Innerchr6:95053242..95169372hg17UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38116131
hg19116131
hg18116131
hg17116131
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517329
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700673
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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