A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612522



Internal ID6999423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22623992..22630344hg38UCSC Ensembl
Innerchr7:22623992..22630344hg38UCSC Ensembl
Outerchr7:22623835..22630469hg38UCSC Ensembl
chr7:22663611..22669963hg19UCSC Ensembl
Innerchr7:22663611..22669963hg19UCSC Ensembl
Outerchr7:22663454..22670088hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg386353
hg196353
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12698576
SamplesNA19130
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612522
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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