A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696404



Internal ID15086370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:121631261..121687538hg38UCSC Ensembl
Innerchr6:121952407..122008684hg19UCSC Ensembl
Innerchr6:121994106..122050383hg18UCSC Ensembl
Innerchr6:121994106..122050383hg17UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3856278
hg1956278
hg1856278
hg1756278
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518938
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696404
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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