A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv872814



Internal ID15820084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46551800..46687409hg38UCSC Ensembl
Innerchr17:44629166..44764775hg19UCSC Ensembl
Innerchr17:41984482..42119955hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38135610
hg19135610
hg18135474
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575384
Supporting Variants
Samples
Known GenesARL17A, ARL17B, LRRC37A2, NSF, NSFP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv872814
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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