A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195114



Internal ID20762154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:53839431..54831270hg38UCSC Ensembl
chr15:54131628..55123468hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38991840
hg19991841
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502530
Supporting Variants
Samples
Known GenesUNC13C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195114
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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