A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574764



Internal ID16362173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36116419..36153146hg38UCSC Ensembl
Innerchr17:34443811..34480526hg19UCSC Ensembl
Innerchr17:31467924..31504639hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3836728
hg1936716
hg1836716
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5535n54
Supporting Variantsnssv869873, nssv869869, nssv869867, nssv869868, nssv869872, nssv869870, nssv869866, nssv869874, nssv869871
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574764
Frequency
Sample Size17421
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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