A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18102043



Internal ID20669083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:49378866..49383250hg38UCSC Ensembl
chr3:49416299..49420683hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg384385
hg194385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6358964
Supporting Variants
Samples
Known GenesRHOA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18102043
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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