A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608039



Internal ID6994970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:8789505..8971020hg38UCSC Ensembl
Innerchr6:8789508..8971017hg38UCSC Ensembl
Outerchr6:8789502..8971023hg38UCSC Ensembl
chr6:8789738..8971253hg19UCSC Ensembl
Innerchr6:8789741..8971250hg19UCSC Ensembl
Outerchr6:8789735..8971256hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38181516
hg19181516
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12184544
SamplesHG01075
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608039
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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