A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515801



Internal ID15442858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:46416208..46443112hg38UCSC Ensembl
Innerchr21:47836122..47863025hg19UCSC Ensembl
Innerchr21:46660550..46687453hg18UCSC Ensembl
Innerchr21:46660550..46687453hg17UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3826905
hg1926904
hg1826904
hg1726904
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv687090, nssv669604, nssv657692, nssv674689, nssv667529, nssv697235, nssv663425, nssv661043, nssv666195, nssv666925, nssv664825, nssv665273, nssv674637, nssv655007, nssv665651, nssv685894, nssv660441, nssv661542, nssv678574
Samples
Known GenesPCNT
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515801
Frequency
Sample Size2026
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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