A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611588



Internal ID6998494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:164133438..164137040hg38UCSC Ensembl
Innerchr6:164133477..164137002hg38UCSC Ensembl
Outerchr6:164133400..164137079hg38UCSC Ensembl
chr6:164554470..164558072hg19UCSC Ensembl
Innerchr6:164554509..164558034hg19UCSC Ensembl
Outerchr6:164554432..164558111hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg383603
hg193603
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12626160
SamplesHG03120
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611588
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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