A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574381



Internal ID16361790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:13622203..13635911hg38UCSC Ensembl
Innerchr17:13525520..13539228hg19UCSC Ensembl
Innerchr17:13466245..13479953hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3813709
hg1913709
hg1813709
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5448n54
Supporting Variantsnssv866937, nssv866936
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574381
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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