A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12238141



Internal ID3355139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27277137..27287068hg38UCSC Ensembl
Innerchr6:27277637..27286568hg38UCSC Ensembl
Outerchr6:27276137..27288068hg38UCSC Ensembl
chr6:27244916..27254847hg19UCSC Ensembl
Innerchr6:27245416..27254347hg19UCSC Ensembl
Outerchr6:27243916..27255847hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg389932
hg199932
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3608426
Supporting Variants
SamplesHG03007
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12238141
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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