A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574740



Internal ID16362149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:34843464..34890183hg38UCSC Ensembl
Innerchr17:33170483..33217202hg19UCSC Ensembl
Innerchr17:30194596..30241315hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3846720
hg1946720
hg1846720
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149356
SamplesHGDP00864
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574740
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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