A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192375



Internal ID20759416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78655466..78710949hg38UCSC Ensembl
chr15:78947808..79003291hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3855484
hg1955484
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499306
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192375
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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