A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608185



Internal ID6995115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15914308..15923355hg38UCSC Ensembl
Innerchr6:15914357..15923306hg38UCSC Ensembl
Outerchr6:15914259..15923404hg38UCSC Ensembl
chr6:15914539..15923586hg19UCSC Ensembl
Innerchr6:15914588..15923537hg19UCSC Ensembl
Outerchr6:15914490..15923635hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg389048
hg199048
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12200601
SamplesHG03464
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608185
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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