A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5942505



Internal ID22717943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35007864..35008793hg38UCSC Ensembl
chr15:35300065..35300994hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38930
hg19930
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17371654
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5942505
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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