A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611575



Internal ID6651793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163144131..163146280hg38UCSC Ensembl
Innerchr6:163144164..163146247hg38UCSC Ensembl
Outerchr6:163144098..163146313hg38UCSC Ensembl
chr6:163565163..163567312hg19UCSC Ensembl
Innerchr6:163565196..163567279hg19UCSC Ensembl
Outerchr6:163565130..163567345hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg382150
hg192150
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12623116
SamplesHG02651
Known GenesPACRG
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611575
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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