A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609916



Internal ID6996835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90112331..90113224hg38UCSC Ensembl
Innerchr6:90112355..90113201hg38UCSC Ensembl
Outerchr6:90112308..90113248hg38UCSC Ensembl
chr6:90822050..90822943hg19UCSC Ensembl
Innerchr6:90822074..90822920hg19UCSC Ensembl
Outerchr6:90822027..90822967hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38894
hg19894
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12460046
SamplesNA20753
Known GenesBACH2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609916
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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