A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522979



Internal ID20896340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:11134004..11134601hg38UCSC Ensembl
chr20:11114652..11115249hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38598
hg19598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066291
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522979
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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