A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15191747



Internal ID21330595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125228053..125228053hg38UCSC Ensembl
chr10:126916622..126916622hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3928222
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15191747
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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