A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12199828



Internal ID1689744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15174379..15179378hg38UCSC Ensembl
Innerchr6:15174879..15178878hg38UCSC Ensembl
Outerchr6:15173379..15180378hg38UCSC Ensembl
chr6:15174610..15179609hg19UCSC Ensembl
Innerchr6:15175110..15179109hg19UCSC Ensembl
Outerchr6:15173610..15180609hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg385000
hg195000
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3608165
Supporting Variants
SamplesHG01566
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12199828
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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