A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12704118



Internal ID3793960
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3612555
Supporting Variants
SamplesHG03439
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12704118
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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