A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608161



Internal ID6995091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15086335..15090549hg38UCSC Ensembl
Innerchr6:15086356..15090529hg38UCSC Ensembl
Outerchr6:15086315..15090570hg38UCSC Ensembl
chr6:15086566..15090780hg19UCSC Ensembl
Innerchr6:15086587..15090760hg19UCSC Ensembl
Outerchr6:15086546..15090801hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg384215
hg194215
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1166e214
Supporting Variantsessv12199818
SamplesNA06994
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608161
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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