A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4742923



Internal ID20518908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40050450..40051891hg38UCSC Ensembl
chr15:40342651..40344092hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381442
hg191442
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16280713
Samples
Known GenesSRP14-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4742923
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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