A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612539



Internal ID6999440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23202701..23204140hg38UCSC Ensembl
Innerchr7:23202751..23204090hg38UCSC Ensembl
Outerchr7:23202593..23204248hg38UCSC Ensembl
chr7:23242320..23243759hg19UCSC Ensembl
Innerchr7:23242370..23243709hg19UCSC Ensembl
Outerchr7:23242212..23243867hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg381440
hg191440
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12703847
SamplesNA20531
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612539
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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