A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15191301



Internal ID21330164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130785608..130785608hg38UCSC Ensembl
chr10:132583872..132583872hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3940977
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15191301
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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