A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575660



Internal ID16363069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:54813676..54848141hg38UCSC Ensembl
Innerchr17:52891037..52925502hg19UCSC Ensembl
Innerchr17:50246036..50280501hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3834466
hg1934466
hg1834466
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150568
Samples1780862432_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575660
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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