A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528265



Internal ID20901626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:39142678..39144051hg38UCSC Ensembl
chr20:37771321..37772694hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg381374
hg191374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068881
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528265
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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