A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6319033



Internal ID9760464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:25681317..25682704hg38UCSC Ensembl
Outerchr4:25681280..25682754hg38UCSC Ensembl
Innerchr4:25682939..25684326hg19UCSC Ensembl
Outerchr4:25682902..25684376hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg381475
hg191475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2669717
Supporting Variants
SamplesNA19716
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6319033
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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