A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702504



Internal ID15092470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:14981199..15186710hg38UCSC Ensembl
Innerchr2:15121323..15326834hg19UCSC Ensembl
Innerchr2:15038774..15244285hg18UCSC Ensembl
Innerchr2:15071921..15277432hg17UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38205512
hg19205512
hg18205512
hg17205512
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515567
Supporting Variants
Samples
Known GenesNBAS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702504
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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