A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611403



Internal ID6998312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158745097..158753970hg38UCSC Ensembl
Innerchr6:158745098..158753970hg38UCSC Ensembl
Outerchr6:158745097..158753971hg38UCSC Ensembl
chr6:159166129..159175002hg19UCSC Ensembl
Innerchr6:159166130..159175002hg19UCSC Ensembl
Outerchr6:159166129..159175003hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg388874
hg198874
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12605654, essv12605653
SamplesNA18547, NA18638
Known GenesSYTL3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611403
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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