A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575954



Internal ID16363363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:71371559..71393760hg38UCSC Ensembl
Innerchr17:69367700..69389901hg19UCSC Ensembl
Innerchr17:66879295..66901496hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3822202
hg1922202
hg1822202
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5761n54
Supporting Variantsnssv875928
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575954
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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