A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611778



Internal ID6998682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:368320..405109hg38UCSC Ensembl
chr7:408286..445075hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3836790
hg1936790
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12657811
SamplesHG01797
Known GenesLOC442497
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611778
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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