A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv658171



Internal ID15394823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:13062091..13145476hg38UCSC Ensembl
Innerchr2:13202216..13285601hg19UCSC Ensembl
Innerchr2:13119667..13203052hg18UCSC Ensembl
Innerchr2:13152814..13236199hg17UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3883386
hg1983386
hg1883386
hg1783386
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516862
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv658171
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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