A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574434



Internal ID16361843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:15131524..15155959hg38UCSC Ensembl
Innerchr17:15034841..15059276hg19UCSC Ensembl
Innerchr17:14975566..15000001hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3824436
hg1924436
hg1824436
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5462n54
Supporting Variantsnssv1149736, nssv1149735
SamplesHGDP01288, HGDP01180
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574434
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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