A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12841065



Internal ID4300026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73914894..73916918hg38UCSC Ensembl
Innerchr7:73914894..73916918hg38UCSC Ensembl
Outerchr7:73914558..73917202hg38UCSC Ensembl
chr7:73329224..73331248hg19UCSC Ensembl
Innerchr7:73329224..73331248hg19UCSC Ensembl
Outerchr7:73328888..73331532hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg382025
hg192025
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3613692
Supporting Variants
SamplesHG03858
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12841065
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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