A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610258



Internal ID6997175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:105854452..105865843hg38UCSC Ensembl
Innerchr6:105854502..105865793hg38UCSC Ensembl
Outerchr6:105854402..105865893hg38UCSC Ensembl
chr6:106302327..106313718hg19UCSC Ensembl
Innerchr6:106302377..106313668hg19UCSC Ensembl
Outerchr6:106302277..106313768hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3811392
hg1911392
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12496947
SamplesNA20758
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610258
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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