A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv876846



Internal ID16170802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:79075961..79091723hg38UCSC Ensembl
Innerchr17:77072043..77087805hg19UCSC Ensembl
Innerchr17:74583638..74599400hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3815763
hg1915763
hg1815763
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576103
Supporting Variants
Samples
Known GenesENGASE, RBFOX3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv876846
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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