A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575554



Internal ID16362963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:52488993..52776415hg38UCSC Ensembl
Innerchr17:50566353..50853775hg19UCSC Ensembl
Innerchr17:47921352..48208774hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38287423
hg19287423
hg18287423
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv873541
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575554
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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