A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574629



Internal ID16362038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:26936341..26940496hg38UCSC Ensembl
Innerchr17:25263367..25267522hg19UCSC Ensembl
Innerchr17:22287494..22291649hg18UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg384156
hg194156
hg184156
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5508n54
Supporting Variantsnssv868967
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574629
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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