A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv872597



Internal ID15819867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46347360..46511163hg38UCSC Ensembl
Innerchr17:44424726..44588529hg19UCSC Ensembl
Innerchr17:41780482..41943845hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38163804
hg19163804
hg18163364
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575297
Supporting Variants
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)nssv872597
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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