A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610498



Internal ID6650724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:117604815..117613107hg38UCSC Ensembl
Innerchr6:117604829..117613093hg38UCSC Ensembl
Outerchr6:117604801..117613121hg38UCSC Ensembl
chr6:117925978..117934270hg19UCSC Ensembl
Innerchr6:117925992..117934256hg19UCSC Ensembl
Outerchr6:117925964..117934284hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg388293
hg198293
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12515783
SamplesHG04219
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610498
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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