A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4978n100



Internal ID22791065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:165848129..165983446hg38UCSC Ensembl
chr3:165565917..165701234hg19UCSC Ensembl
chr3:167048611..167183928hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38135318
hg19135318
hg18135318
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv999001, nsv997950
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)dgv4978n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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