A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575286



Internal ID16016009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46337891..46481604hg38UCSC Ensembl
Innerchr17:44415257..44558970hg19UCSC Ensembl
Innerchr17:41771015..41914286hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38143714
hg19143714
hg18143272
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5641n54
Supporting Variantsnssv872574, nssv872575
Samples
Known GenesARL17A, ARL17B, NSFP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575286
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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