A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694668



Internal ID15431320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:100675627..100711074hg38UCSC Ensembl
Innerchr6:101123503..101158950hg19UCSC Ensembl
Innerchr6:101230224..101265671hg18UCSC Ensembl
Innerchr6:101230224..101265671hg17UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3835448
hg1935448
hg1835448
hg1735448
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521897
Supporting Variants
Samples
Known GenesASCC3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694668
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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