A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576097



Internal ID16016820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:78464855..78602041hg38UCSC Ensembl
Innerchr17:76460937..76598123hg19UCSC Ensembl
Innerchr17:73972532..74109718hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38137187
hg19137187
hg18137187
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv876843
Samples
Known GenesDNAH17, DNAH17-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576097
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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