A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611327



Internal ID6998236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154739085..154741656hg38UCSC Ensembl
Innerchr6:154739085..154741656hg38UCSC Ensembl
Outerchr6:154738765..154741962hg38UCSC Ensembl
chr6:155060219..155062790hg19UCSC Ensembl
Innerchr6:155060219..155062790hg19UCSC Ensembl
Outerchr6:155059899..155063096hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg382572
hg192572
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12594529, essv12594530
SamplesHG04096, HG03717
Known GenesSCAF8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611327
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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