A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612306



Internal ID6652520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:14021744..14237390hg38UCSC Ensembl
chr7:14061369..14277015hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg38215647
hg19215647
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12685453, essv12685454, essv12685452, essv12685455
SamplesNA19020, NA18634, NA19321, NA20276
Known GenesDGKB
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612306
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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