A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4748065



Internal ID20524089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44857549..45026631hg38UCSC Ensembl
chr15:45149747..45318829hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38169083
hg19169083
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16290432
Samples
Known GenesC15orf43, SORD
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4748065
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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