A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612555



Internal ID6999455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23867207..23875743hg38UCSC Ensembl
Innerchr7:23867219..23875731hg38UCSC Ensembl
Outerchr7:23867195..23875755hg38UCSC Ensembl
chr7:23906826..23915362hg19UCSC Ensembl
Innerchr7:23906838..23915350hg19UCSC Ensembl
Outerchr7:23906814..23915374hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg388537
hg198537
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12704118
SamplesHG03439
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612555
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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