A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614386



Internal ID6654592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:104096478..104186166hg38UCSC Ensembl
chr7:103736925..103826614hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3889689
hg1989690
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12913147
SamplesNA19783
Known GenesORC5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614386
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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