A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615019



Internal ID7001908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:130239988..130243311hg38UCSC Ensembl
Innerchr7:130240016..130243284hg38UCSC Ensembl
Outerchr7:130239961..130243339hg38UCSC Ensembl
chr7:129879828..129883151hg19UCSC Ensembl
Innerchr7:129879856..129883124hg19UCSC Ensembl
Outerchr7:129879801..129883179hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg383324
hg193324
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12971916
SamplesHG00240
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615019
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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