A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611747



Internal ID6651965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:78321..231876hg38UCSC Ensembl
chr7:78321..231876hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38153556
hg19153556
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12656620, essv12656621
SamplesNA19731, HG01797
Known GenesFAM20C, LOC100507642
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611747
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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