A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18099969



Internal ID20667009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4357624..4360917hg38UCSC Ensembl
chr3:4399308..4402601hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg383294
hg193294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367212
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18099969
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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