A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575557



Internal ID16362966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:52738675..52867221hg38UCSC Ensembl
Innerchr17:50816035..50944581hg19UCSC Ensembl
Innerchr17:48171034..48299580hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38128547
hg19128547
hg18128547
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv873544
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575557
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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