A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615203



Internal ID7002092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138828034..138830776hg38UCSC Ensembl
Innerchr7:138828095..138830716hg38UCSC Ensembl
Outerchr7:138827974..138830837hg38UCSC Ensembl
chr7:138512779..138515521hg19UCSC Ensembl
Innerchr7:138512840..138515461hg19UCSC Ensembl
Outerchr7:138512719..138515582hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg382743
hg192743
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12981858, essv12981857
SamplesHG03826, HG04195
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615203
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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