A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18099151



Internal ID20666191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:40610433..40618286hg38UCSC Ensembl
chr3:40651924..40659777hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg387854
hg197854
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6360774
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18099151
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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