A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516919



Internal ID15097526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:125942455..125955813hg38UCSC Ensembl
Innerchr11:125812350..125825708hg19UCSC Ensembl
Innerchr11:125317560..125330918hg18UCSC Ensembl
Innerchr11:125317560..125330918hg17UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3813359
hg1913359
hg1813359
hg1713359
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv691217, nssv663571, nssv654986, nssv692603, nssv699931, nssv698963
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516919
Frequency
Sample Size2026
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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