A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17518571



Internal ID21842930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19519073..19519292hg38UCSC Ensembl
chr1:19845567..19845786hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38220
hg19220
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5982156
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17518571
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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