A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4731356



Internal ID20507276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36662468..36662520hg38UCSC Ensembl
chr15:36954669..36954721hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16277823
Samples
Known GenesC15orf41
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4731356
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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