A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609258



Internal ID6996180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63351122..63352113hg38UCSC Ensembl
Innerchr6:63351140..63352096hg38UCSC Ensembl
Outerchr6:63351105..63352131hg38UCSC Ensembl
chr6:64061027..64062018hg19UCSC Ensembl
Innerchr6:64061045..64062001hg19UCSC Ensembl
Outerchr6:64061010..64062036hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38992
hg19992
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12389792
SamplesHG02343
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609258
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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