A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18069153



Internal ID20636193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:59498701..59501000hg38UCSC Ensembl
chr20:58073756..58076055hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6546943
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18069153
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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