A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611346



Internal ID6998255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:155512406..155520443hg38UCSC Ensembl
Innerchr6:155512422..155520428hg38UCSC Ensembl
Outerchr6:155512391..155520459hg38UCSC Ensembl
chr6:155833540..155841577hg19UCSC Ensembl
Innerchr6:155833556..155841562hg19UCSC Ensembl
Outerchr6:155833525..155841593hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg388038
hg198038
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12596971, essv12596970, essv12596967, essv12596969, essv12596968
SamplesHG02702, HG03298, HG02813, HG01105, HG02343
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611346
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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