A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610099



Internal ID6997018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:98031388..98039326hg38UCSC Ensembl
Innerchr6:98031407..98039308hg38UCSC Ensembl
Outerchr6:98031370..98039345hg38UCSC Ensembl
chr6:98479264..98487202hg19UCSC Ensembl
Innerchr6:98479283..98487184hg19UCSC Ensembl
Outerchr6:98479246..98487221hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg387939
hg197939
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12474934
SamplesHG00383
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610099
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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