A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4991n100



Internal ID22791078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:176173010..176219130hg38UCSC Ensembl
chr3:175890798..175936918hg19UCSC Ensembl
chr3:177373492..177419612hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3846121
hg1946121
hg1846121
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1010962, nsv998195, nsv1013158, nsv1012425, nsv1006280, nsv999585
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)dgv4991n100
Frequency
Sample Size11257
Observed Gain17
Observed Loss0
Observed Complex0
Frequencyn/a


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