A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15747469



Internal ID21388611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:9957984..9962421hg38UCSC Ensembl
chr20:9938632..9943069hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg384438
hg194438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4433323
Supporting Variants
SamplesNB08
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15747469
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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