A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv872823



Internal ID15820093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46565999..46610400hg38UCSC Ensembl
Innerchr17:44643365..44687766hg19UCSC Ensembl
Innerchr17:41998681..42043082hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3844402
hg1944402
hg1844402
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575390
Supporting Variants
Samples
Known GenesARL17A, ARL17B, NSF, NSFP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv872823
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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