A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589650



Internal ID16030373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:10260488..10294102hg38UCSC Ensembl
Innerchr3:10302172..10335786hg19UCSC Ensembl
Innerchr3:10277172..10310786hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3833615
hg1933615
hg1833615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151867
Samples1780854295_A
Known GenesGHRL, GHRLOS, LINC00852, TATDN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589650
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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