A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18096052



Internal ID20663092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153270398..153279027hg38UCSC Ensembl
chr3:152988187..152996816hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg388630
hg198630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6372962
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18096052
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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