A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515904



Internal ID15442961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:24997095..25005198hg38UCSC Ensembl
Innerchr13:25571233..25579336hg19UCSC Ensembl
Innerchr13:24469233..24477336hg18UCSC Ensembl
Innerchr13:24469233..24477336hg17UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg388104
hg198104
hg188104
hg178104
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv106n21
Supporting Variantsnssv687023, nssv679191, nssv677863, nssv654283, nssv661489, nssv668808, nssv656326, nssv687320, nssv680879, nssv654467, nssv677357, nssv665219, nssv657295, nssv669655, nssv657158
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515904
Frequency
Sample Size2026
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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