A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608884



Internal ID6995808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:46398743..46400551hg38UCSC Ensembl
Innerchr6:46398765..46400529hg38UCSC Ensembl
Outerchr6:46398721..46400573hg38UCSC Ensembl
chr6:46366480..46368288hg19UCSC Ensembl
Innerchr6:46366502..46368266hg19UCSC Ensembl
Outerchr6:46366458..46368310hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg381809
hg191809
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12341401
SamplesHG04202
Known GenesRCAN2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608884
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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