A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697332



Internal ID15433984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:37392781..37412548hg38UCSC Ensembl
Innerchr6:37360557..37380324hg19UCSC Ensembl
Innerchr6:37468535..37488302hg18UCSC Ensembl
Innerchr6:37468535..37488302hg17UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3819768
hg1919768
hg1819768
hg1719768
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520294
Supporting Variants
Samples
Known GenesRNF8
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697332
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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