A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574314



Internal ID16361723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:6194574..6227773hg38UCSC Ensembl
Innerchr17:6097894..6131093hg19UCSC Ensembl
Innerchr17:6038618..6071817hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3833200
hg1933200
hg1833200
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5438n54
Supporting Variantsnssv866662
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574314
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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