A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576099



Internal ID16016822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:78577234..78599049hg38UCSC Ensembl
Innerchr17:76573316..76595131hg19UCSC Ensembl
Innerchr17:74084911..74106726hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3821816
hg1921816
hg1821816
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5789n54
Supporting Variantsnssv876844
Samples
Known GenesDNAH17
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576099
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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