A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575573



Internal ID16362982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:53373203..53501617hg38UCSC Ensembl
Innerchr17:51450564..51578978hg19UCSC Ensembl
Innerchr17:48805563..48933977hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38128415
hg19128415
hg18128415
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5694n54
Supporting Variantsnssv873557
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575573
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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