A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574990



Internal ID16015713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:38704414..38705443hg38UCSC Ensembl
Innerchr17:36860667..36861696hg19UCSC Ensembl
Innerchr17:34114193..34115222hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381030
hg191030
hg181030
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv870532
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574990
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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