A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524219



Internal ID20897580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33811201..33811700hg38UCSC Ensembl
chr20:32399007..32399506hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067465
Samples
Known GenesCHMP4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524219
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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