A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18067870



Internal ID20634910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53549927..53552510hg38UCSC Ensembl
chr20:52166466..52169049hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg382584
hg192584
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536855
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18067870
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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