A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv872580



Internal ID15819850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46342566..46489976hg38UCSC Ensembl
Innerchr17:44419932..44567342hg19UCSC Ensembl
Innerchr17:41775690..41922658hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38147411
hg19147411
hg18146969
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575289
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)nssv872580
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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