A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16295605



Internal ID20504823
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 StatusS
Merged Variantsnsv4757501
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16295605
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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