A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610370



Internal ID6997287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110914754..110919578hg38UCSC Ensembl
Innerchr6:110914792..110919540hg38UCSC Ensembl
Outerchr6:110914716..110919616hg38UCSC Ensembl
chr6:111235957..111240781hg19UCSC Ensembl
Innerchr6:111235995..111240743hg19UCSC Ensembl
Outerchr6:111235919..111240819hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg384825
hg194825
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12503613
SamplesNA19137
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610370
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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