A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611418



Internal ID6998327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159522418..159529467hg38UCSC Ensembl
Innerchr6:159522447..159529438hg38UCSC Ensembl
Outerchr6:159522389..159529496hg38UCSC Ensembl
chr6:159943450..159950499hg19UCSC Ensembl
Innerchr6:159943479..159950470hg19UCSC Ensembl
Outerchr6:159943421..159950528hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg387050
hg197050
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12608425
SamplesHG04211
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611418
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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