A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609072



Internal ID6995995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:55606298..55612728hg38UCSC Ensembl
Innerchr6:55606298..55612728hg38UCSC Ensembl
Outerchr6:55606133..55612885hg38UCSC Ensembl
chr6:55471096..55477526hg19UCSC Ensembl
Innerchr6:55471096..55477526hg19UCSC Ensembl
Outerchr6:55470931..55477683hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg386431
hg196431
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12363356
SamplesHG01051
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609072
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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