A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528565



Internal ID15455858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:14356322..14370010hg38UCSC Ensembl
Innerchr2:14496446..14510134hg19UCSC Ensembl
Innerchr2:14413897..14427585hg18UCSC Ensembl
Innerchr2:14447044..14460732hg17UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3813689
hg1913689
hg1813689
hg1713689
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705181
Samples
Known GenesLINC00276
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528565
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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