A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192429



Internal ID20759470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:116640403..116651507hg38UCSC Ensembl
chr10:118399914..118411018hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3811105
hg1911105
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449016
Supporting Variants
Samples
Known GenesPNLIPRP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192429
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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