A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609919



Internal ID6996838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90282284..90293936hg38UCSC Ensembl
Innerchr6:90282284..90293936hg38UCSC Ensembl
Outerchr6:90281784..90294436hg38UCSC Ensembl
chr6:90992003..91003655hg19UCSC Ensembl
Innerchr6:90992003..91003655hg19UCSC Ensembl
Outerchr6:90991503..91004155hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3811653
hg1911653
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12460057
SamplesHG03539
Known GenesBACH2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609919
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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