A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5945785



Internal ID22721266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49880094..49906469hg38UCSC Ensembl
chr15:50172291..50198666hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3826376
hg1926376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17372358
Samples
Known GenesATP8B4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5945785
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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