A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4741196



Internal ID20517173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35656414..35656543hg38UCSC Ensembl
chr15:35948615..35948744hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267934
Samples
Known GenesDPH6-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4741196
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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