A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611862



Internal ID6998764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:3076499..3140840hg38UCSC Ensembl
chr7:3116133..3180474hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3864342
hg1964342
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12669733, essv12669732
SamplesNA18560, HG00653
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611862
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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