A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695960



Internal ID15432612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:227376050..227402392hg38UCSC Ensembl
Innerchr2:228240766..228267108hg19UCSC Ensembl
Innerchr2:227949010..227975352hg18UCSC Ensembl
Innerchr2:228066271..228092613hg17UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg3826343
hg1926343
hg1826343
hg1726343
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518519
Supporting Variants
Samples
Known GenesTM4SF20
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695960
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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