A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610410



Internal ID6997327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:113323914..113330243hg38UCSC Ensembl
Innerchr6:113323914..113330243hg38UCSC Ensembl
Outerchr6:113323681..113330364hg38UCSC Ensembl
chr6:113645116..113651445hg19UCSC Ensembl
Innerchr6:113645116..113651445hg19UCSC Ensembl
Outerchr6:113644883..113651566hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg386330
hg196330
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1211e214
Supporting Variantsessv12505915, essv12505917, essv12505916
SamplesHG01443, HG01134, HG01550
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610410
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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