A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17395601



Internal ID22453471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:22378416..22378473hg38UCSC Ensembl
chr20:22359054..22359111hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5958205
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17395601
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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