A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612621



Internal ID6652834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26104867..26159628hg38UCSC Ensembl
chr7:26144487..26199248hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3854762
hg1954762
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12710359
SamplesHG02006
Known GenesNFE2L3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612621
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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