A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608190



Internal ID6995120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:16218019..16226643hg38UCSC Ensembl
Innerchr6:16218019..16226643hg38UCSC Ensembl
Outerchr6:16217998..16226685hg38UCSC Ensembl
chr6:16218250..16226874hg19UCSC Ensembl
Innerchr6:16218250..16226874hg19UCSC Ensembl
Outerchr6:16218229..16226916hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg388625
hg198625
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12200613
SamplesNA19749
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608190
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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