A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576104



Internal ID16363513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:79161021..79187082hg38UCSC Ensembl
Innerchr17:77157103..77183164hg19UCSC Ensembl
Innerchr17:74668698..74694759hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3826062
hg1926062
hg1826062
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv876847
Samples
Known GenesRBFOX3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576104
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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