A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612628



Internal ID6652841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26179273..26181724hg38UCSC Ensembl
Innerchr7:26179273..26181724hg38UCSC Ensembl
Outerchr7:26179051..26181977hg38UCSC Ensembl
chr7:26218893..26221344hg19UCSC Ensembl
Innerchr7:26218893..26221344hg19UCSC Ensembl
Outerchr7:26218671..26221597hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg382452
hg192452
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12710380, essv12710381
SamplesHG01107, NA18858
Known GenesNFE2L3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612628
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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