A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17353883



Internal ID22579552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:22323772..22326081hg38UCSC Ensembl
chr1:22650265..22652574hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg382310
hg192310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5867693
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17353883
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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