A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575373



Internal ID16016096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46463467..46526639hg38UCSC Ensembl
Innerchr17:44540833..44604005hg19UCSC Ensembl
Innerchr17:41896148..41959321hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3863173
hg1963173
hg1863174
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5656n54
Supporting Variantsnssv872795
Samples
Known GenesARL17A, LRRC37A2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575373
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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