A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610462



Internal ID6997379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:115848593..115898207hg38UCSC Ensembl
Innerchr6:115848593..115898207hg38UCSC Ensembl
Outerchr6:115848093..115898707hg38UCSC Ensembl
chr6:116169757..116219371hg19UCSC Ensembl
Innerchr6:116169757..116219371hg19UCSC Ensembl
Outerchr6:116169257..116219871hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg3849615
hg1949615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12509692
SamplesNA07037
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610462
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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