A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12566239



Internal ID2568055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:139181692..139190501hg38UCSC Ensembl
Innerchr6:139181692..139190501hg38UCSC Ensembl
Outerchr6:139181458..139190745hg38UCSC Ensembl
chr6:139502829..139511638hg19UCSC Ensembl
Innerchr6:139502829..139511638hg19UCSC Ensembl
Outerchr6:139502595..139511882hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg388810
hg198810
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3610967
Supporting Variants
SamplesHG03354
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12566239
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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