A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18100337



Internal ID20667377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:23046701..23050400hg38UCSC Ensembl
chr3:23088192..23091891hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg383700
hg193700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6371497
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18100337
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00727


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