A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12503903



Internal ID2505719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110973969..110983882hg38UCSC Ensembl
Innerchr6:110974469..110983382hg38UCSC Ensembl
Outerchr6:110972969..110984882hg38UCSC Ensembl
chr6:111295172..111305085hg19UCSC Ensembl
Innerchr6:111295672..111304585hg19UCSC Ensembl
Outerchr6:111294172..111306085hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg389914
hg199914
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3610372
Supporting Variants
SamplesHG01566
Known GenesRPF2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12503903
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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