A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002987



Internal ID19092204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:152155931..152188504hg38UCSC Ensembl
Innerchr3:151873720..151906293hg19UCSC Ensembl
Innerchr3:153356410..153388983hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3832574
hg1932574
hg1832574
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3741540
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1002987
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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