A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014557



Internal ID18757092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:158458793..158533813hg38UCSC Ensembl
Innerchr3:158176582..158251602hg19UCSC Ensembl
Innerchr3:159659276..159734296hg18UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg3875021
hg1975021
hg1875021
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4929n100
Supporting Variantsnssv3606392
Samples
Known GenesRSRC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014557
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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