A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026075



Internal ID20593115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:61249433..61249956hg38UCSC Ensembl
chr15:61541632..61542155hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38524
hg19524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513461
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026075
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00037


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