A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528747



Internal ID20902108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:39160574..39161238hg38UCSC Ensembl
chr20:37789217..37789881hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38665
hg19665
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068882
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528747
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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