A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18065773



Internal ID20632813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:97952227..97952584hg38UCSC Ensembl
chr1:98417783..98418140hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38358
hg19358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6325715
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18065773
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00218


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