A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609717



Internal ID6996637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:80637662..80667173hg38UCSC Ensembl
Innerchr6:80637662..80667173hg38UCSC Ensembl
Outerchr6:80637162..80667673hg38UCSC Ensembl
chr6:81347379..81376890hg19UCSC Ensembl
Innerchr6:81347379..81376890hg19UCSC Ensembl
Outerchr6:81346879..81377390hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3829512
hg1929512
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12449917
SamplesHG02136
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609717
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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