A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12707802



Internal ID4243803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24486279..24498229hg38UCSC Ensembl
Innerchr7:24486279..24498229hg38UCSC Ensembl
Outerchr7:24486081..24498333hg38UCSC Ensembl
chr7:24525898..24537848hg19UCSC Ensembl
Innerchr7:24525898..24537848hg19UCSC Ensembl
Outerchr7:24525700..24537952hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3811951
hg1911951
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3612583
Supporting Variants
SamplesHG03815
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12707802
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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