A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17380354



Internal ID22438224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58496912..58497228hg38UCSC Ensembl
chr15:58789111..58789427hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5947052
Supporting Variants
Samples
Known GenesLIPC
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17380354
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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