A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611858



Internal ID6652073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2921683..3274709hg38UCSC Ensembl
chr7:2961317..3314341hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg38353027
hg19353025
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12668873, essv12668872
SamplesNA18560, HG00653
Known GenesCARD11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611858
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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