A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13033263



Internal ID1592864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155266083..155288332hg38UCSC Ensembl
Innerchr7:155266083..155288332hg38UCSC Ensembl
Outerchr7:155265583..155288832hg38UCSC Ensembl
chr7:155057793..155080042hg19UCSC Ensembl
Innerchr7:155057793..155080042hg19UCSC Ensembl
Outerchr7:155057293..155080542hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3822250
hg1922250
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3615627
Supporting Variants
SamplesHG01479
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13033263
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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