A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611417



Internal ID6998326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159493448..159497297hg38UCSC Ensembl
Innerchr6:159493448..159497297hg38UCSC Ensembl
Outerchr6:159493271..159497469hg38UCSC Ensembl
chr6:159914480..159918329hg19UCSC Ensembl
Innerchr6:159914480..159918329hg19UCSC Ensembl
Outerchr6:159914303..159918501hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg383850
hg193850
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12608423, essv12608424, essv12608422
SamplesHG03862, HG04155, HG03238
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611417
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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