A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609651



Internal ID6996572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:78092557..78149661hg38UCSC Ensembl
Innerchr6:78092580..78149639hg38UCSC Ensembl
Outerchr6:78092535..78149684hg38UCSC Ensembl
chr6:78802274..78859378hg19UCSC Ensembl
Innerchr6:78802297..78859356hg19UCSC Ensembl
Outerchr6:78802252..78859401hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3857105
hg1957105
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12442962
SamplesHG01980
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609651
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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