A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575840



Internal ID16363249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:61534680..61569403hg38UCSC Ensembl
Innerchr17:59612041..59646764hg19UCSC Ensembl
Innerchr17:56966823..57001546hg18UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3834724
hg1934724
hg1834724
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149779
SamplesHGDP00580
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575840
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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