A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5940515



Internal ID22715925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73646299..73648728hg38UCSC Ensembl
chr15:73938640..73941069hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg382430
hg192430
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17377750
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5940515
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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