A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5944350



Internal ID22719814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78928327..78941551hg38UCSC Ensembl
chr15:79220669..79233893hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3813225
hg1913225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17383643
Samples
Known GenesCTSH
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5944350
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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