A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv960e214



Internal ID20122383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183134096..183206174hg38UCSC Ensembl
chr3:182851884..182923962hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg3872079
hg1972079
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3598920, esv3598921, esv3598919
SamplesHG03061, NA19390
Known GenesLAMP3, MCF2L2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv960e214
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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