A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610486



Internal ID6997403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:117175309..117258293hg38UCSC Ensembl
chr6:117496472..117579456hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg3882985
hg1982985
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12513048, essv12513050, essv12513049
SamplesNA18861, HG03091, HG03538
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610486
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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