A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5942626



Internal ID22718067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52104739..52107648hg38UCSC Ensembl
chr15:52396936..52399845hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg382910
hg192910
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389141
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5942626
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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