A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574677



Internal ID16362086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:31751698..31789827hg38UCSC Ensembl
Innerchr17:30078717..30116846hg19UCSC Ensembl
Innerchr17:27102830..27140959hg18UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3838130
hg1938130
hg1838130
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149354
SamplesHGDP00752
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574677
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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