A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574665



Internal ID16362074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:30860479..30880727hg38UCSC Ensembl
Innerchr17:29187497..29207745hg19UCSC Ensembl
Innerchr17:26211623..26231871hg18UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3820249
hg1920249
hg1820249
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5519n54
Supporting Variantsnssv869520
Samples
Known GenesATAD5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574665
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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