A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661538



Internal ID15398190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:13052619..13142111hg38UCSC Ensembl
Innerchr2:13192744..13282236hg19UCSC Ensembl
Innerchr2:13110195..13199687hg18UCSC Ensembl
Innerchr2:13143342..13232834hg17UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3889493
hg1989493
hg1889493
hg1789493
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)nssv661538
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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