A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612519



Internal ID6999420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22407079..22414064hg38UCSC Ensembl
Innerchr7:22407098..22414045hg38UCSC Ensembl
Outerchr7:22407060..22414083hg38UCSC Ensembl
chr7:22446698..22453683hg19UCSC Ensembl
Innerchr7:22446717..22453664hg19UCSC Ensembl
Outerchr7:22446679..22453702hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg386986
hg196986
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12698571, essv12698572
SamplesHG00689, HG00692
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612519
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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