A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12860922



Internal ID2021447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:79871951..79976802hg38UCSC Ensembl
chr7:79501267..79606118hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38104852
hg19104852
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3613843
Supporting Variants
SamplesHG01861
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12860922
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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