A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18025100



Internal ID20592140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:54345019..54345514hg38UCSC Ensembl
chr15:54637217..54637712hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38496
hg19496
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500999
Supporting Variants
Samples
Known GenesUNC13C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18025100
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00055


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