A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519631



Internal ID15100238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3752639..3778345hg38UCSC Ensembl
Innerchr4:3754366..3780072hg19UCSC Ensembl
Innerchr4:3724164..3749870hg18UCSC Ensembl
Innerchr4:3791335..3817041hg17UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg3825707
hg1925707
hg1825707
hg1725707
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv692220, nssv690271, nssv677580, nssv657243, nssv676876, nssv660187, nssv678280, nssv688688
Samples
Known GenesADRA2C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519631
Frequency
Sample Size2026
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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