A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4721n100



Internal ID22790808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37933317..37945639hg38UCSC Ensembl
chr3:37974808..37987130hg19UCSC Ensembl
chr3:37949812..37962134hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3812323
hg1912323
hg1812323
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1005998, nsv1013731, nsv1001035, nsv1001179, nsv1009721, nsv1000128, nsv1007951
Samples
Known GenesCTDSPL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4721n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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