A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575335



Internal ID16016058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46358514..46474910hg38UCSC Ensembl
Innerchr17:44435880..44552276hg19UCSC Ensembl
Innerchr17:41791622..41907592hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38116397
hg19116397
hg18115971
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5645n54
Supporting Variantsnssv872705
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)nsv575335
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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