A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696886



Internal ID15086852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:36948130..36956326hg38UCSC Ensembl
Innerchr6:36915906..36924102hg19UCSC Ensembl
Innerchr6:37023884..37032080hg18UCSC Ensembl
Innerchr6:37023884..37032080hg17UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg388197
hg198197
hg188197
hg178197
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519499
Supporting Variants
Samples
Known GenesPI16
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696886
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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