A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608139



Internal ID6995069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13849588..13864244hg38UCSC Ensembl
Innerchr6:13850088..13863744hg38UCSC Ensembl
Outerchr6:13848588..13865244hg38UCSC Ensembl
chr6:13849819..13864475hg19UCSC Ensembl
Innerchr6:13850319..13863975hg19UCSC Ensembl
Outerchr6:13848819..13865475hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3814657
hg1914657
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12195954
SamplesNA19066
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608139
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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