A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575920



Internal ID16016643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:67993468..67994171hg38UCSC Ensembl
Innerchr17:65989584..65990287hg19UCSC Ensembl
Innerchr17:63420046..63420749hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38704
hg19704
hg18704
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5755n54
Supporting Variantsnssv875901
Samples
Known GenesC17orf58
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575920
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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