A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520638



Internal ID15101245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:26169872..26190499hg38UCSC Ensembl
Innerchr2:26392741..26413368hg19UCSC Ensembl
Innerchr2:26246245..26266872hg18UCSC Ensembl
Innerchr2:26304392..26325019hg17UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3820628
hg1920628
hg1820628
hg1720628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703509, nssv673404, nssv679232, nssv688662
Samples
Known GenesGAREML
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520638
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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