A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524535



Internal ID15451828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:77083471..77117526hg38UCSC Ensembl
Innerchr2:77310597..77344652hg19UCSC Ensembl
Innerchr2:77164105..77198160hg18UCSC Ensembl
Innerchr2:77222252..77256307hg17UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3834056
hg1934056
hg1834056
hg1734056
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700485
Samples
Known GenesLRRTM4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524535
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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