A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612626



Internal ID6652839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26149311..26183188hg38UCSC Ensembl
chr7:26188931..26222808hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3833878
hg1933878
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12710377, essv12710378
SamplesHG02006, HG02186
Known GenesNFE2L3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612626
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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