A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757501



Internal ID20533361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36132563..36132563hg38UCSC Ensembl
chr15:36424764..36424764hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295605
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757501
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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