A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4929n100



Internal ID20156545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:158458793..158533813hg38UCSC Ensembl
chr3:158176582..158251602hg19UCSC Ensembl
chr3:159659276..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 Variants
Supporting Variantsnsv1013046, nsv1014557
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)dgv4929n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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