A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4921n100



Internal ID20156537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151790048..151825513hg38UCSC Ensembl
chr3:151507836..151543301hg19UCSC Ensembl
chr3:152990526..153025991hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3835466
hg1935466
hg1835466
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1006257, nsv1006083, nsv1005836, nsv1000682, nsv1011550, nsv1004921, nsv1006960, nsv1002095, nsv999101
Samples
Known GenesAADAC, MIR548H2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4921n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss148
Observed Complex0
Frequencyn/a


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