A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610843



Internal ID6651069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132752877..132755889hg38UCSC Ensembl
Innerchr6:132752901..132755866hg38UCSC Ensembl
Outerchr6:132752854..132755913hg38UCSC Ensembl
chr6:133074016..133077028hg19UCSC Ensembl
Innerchr6:133074040..133077005hg19UCSC Ensembl
Outerchr6:133073993..133077052hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg383013
hg193013
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12554759, essv12554758
SamplesNA21130, NA19072
Known GenesVNN2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610843
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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