A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15193837



Internal ID21332727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96541061..96541061hg38UCSC Ensembl
chr15:97084291..97084291hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3945231
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15193837
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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