A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528660



Internal ID20902021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:20130032..20330146hg38UCSC Ensembl
chr20:20110676..20310790hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38200115
hg19200115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067022
Samples
Known GenesC20orf26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528660
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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