A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574378



Internal ID16361787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:13621600..13635911hg38UCSC Ensembl
Innerchr17:13524917..13539228hg19UCSC Ensembl
Innerchr17:13465642..13479953hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3814312
hg1914312
hg1814312
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5448n54
Supporting Variantsnssv866930
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574378
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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