A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611398



Internal ID6998307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158530809..158533698hg38UCSC Ensembl
Innerchr6:158530866..158533641hg38UCSC Ensembl
Outerchr6:158530752..158533755hg38UCSC Ensembl
chr6:158951841..158954730hg19UCSC Ensembl
Innerchr6:158951898..158954673hg19UCSC Ensembl
Outerchr6:158951784..158954787hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg382890
hg192890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12605642, essv12605647, essv12605640, essv12605643, essv12605646, essv12605641, essv12605639, essv12605645, essv12605644
SamplesNA20771, NA12005, HG03817, HG02493, HG03968, HG02736, HG02737, HG01086, HG01097
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611398
Frequency
Sample Size2504
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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