A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526784



Internal ID20900145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32506879..32507123hg38UCSC Ensembl
chr20:31094682..31094926hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38245
hg19245
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067395
Samples
Known GenesC20orf112
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526784
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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