A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5590996



Internal ID21539568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79512291..79512649hg38UCSC Ensembl
chr15:79804633..79804991hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38359
hg19359
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17081278
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5590996
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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