A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17603691



Internal ID21795738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83342135..83342135hg38UCSC Ensembl
chr15:84010887..84010887hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6087827
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17603691
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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