A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18023144



Internal ID20590185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99352501..99354800hg38UCSC Ensembl
chr14:99818838..99821137hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500740
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18023144
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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