A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574132



Internal ID16361541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:949100..949747hg38UCSC Ensembl
Innerchr17:852340..852987hg19UCSC Ensembl
Innerchr17:799090..799737hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38648
hg19648
hg18648
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5398n54
Supporting Variantsnssv866215, nssv866207, nssv866223, nssv866205, nssv866214, nssv866228, nssv866213, nssv866210, nssv866226, nssv866218, nssv866217, nssv866221, nssv866212, nssv866219, nssv866216, nssv866199, nssv866229, nssv866208, nssv866224, nssv866204, nssv866200, nssv866211, nssv866222, nssv866203, nssv866202, nssv866220, nssv866227, nssv866201, nssv866206, nssv866225, nssv866209
Samples
Known GenesNXN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574132
Frequency
Sample Size17421
Observed Gain0
Observed Loss31
Observed Complex0
Frequencyn/a


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