A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935252



Internal ID22710591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34040620..34041105hg38UCSC Ensembl
chr15:34332821..34333306hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38486
hg19486
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17371351
Samples
Known GenesCHRM5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935252
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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