A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4931n100



Internal ID22791018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:161692892..161834469hg38UCSC Ensembl
chr3:161410680..161552257hg19UCSC Ensembl
chr3:162893374..163034951hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38141578
hg19141578
hg18141578
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1002053, nsv1001318, nsv1008832, nsv1012945, nsv1003495, nsv1008088, nsv1012052
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)dgv4931n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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