A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611787



Internal ID6998691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:791320..794061hg38UCSC Ensembl
Innerchr7:791330..794051hg38UCSC Ensembl
Outerchr7:791310..794071hg38UCSC Ensembl
chr7:830957..833698hg19UCSC Ensembl
Innerchr7:830967..833688hg19UCSC Ensembl
Outerchr7:830947..833708hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg382742
hg192742
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12657951, essv12657950, essv12657952
SamplesNA20514, NA19149, HG03039
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611787
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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