A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575571



Internal ID16362980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:53255898..53361584hg38UCSC Ensembl
Innerchr17:51333259..51438945hg19UCSC Ensembl
Innerchr17:48688258..48793944hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38105687
hg19105687
hg18105687
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149773
SamplesHGDP00226
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575571
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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