A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17388218



Internal ID22446088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51381547..51381678hg38UCSC Ensembl
chr15:51673744..51673875hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5944799
Supporting Variants
Samples
Known GenesGLDN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17388218
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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