A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615214



Internal ID7002103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139493880..139508650hg38UCSC Ensembl
chr7:139178626..139193396hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3814771
hg1914771
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12982066, essv12982064, essv12982065
SamplesHG02890, HG03382, HG03410
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615214
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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