A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv876910



Internal ID16170866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:80711376..80744868hg38UCSC Ensembl
Innerchr17:78685176..78718668hg19UCSC Ensembl
Innerchr17:76299771..76333263hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3833493
hg1933493
hg1833493
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576140
Supporting Variants
Samples
Known GenesRPTOR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv876910
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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