A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18025542



Internal ID20592583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:54576557..54576938hg38UCSC Ensembl
chr15:54868755..54869136hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38382
hg19382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498732
Supporting Variants
Samples
Known GenesUNC13C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18025542
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0015


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