A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007981



Internal ID19097200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:87900166..87954886hg38UCSC Ensembl
Innerchr3:87949316..88004036hg19UCSC Ensembl
Innerchr3:88032006..88086726hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3854721
hg1954721
hg1854721
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3596279
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)nsv1007981
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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