A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv961e214



Internal ID20122384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184286928..184306834hg38UCSC Ensembl
chr3:184004716..184024622hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg3819907
hg1919907
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3598941, esv3598942
SamplesHG03061, HG00672, HG00255
Known GenesECE2, PSMD2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv961e214
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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