A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15195437



Internal ID21334345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90871538..90871538hg38UCSC Ensembl
chr15:91414768..91414768hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38347
hg19347
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3928711
Supporting Variants
SamplesHG002
Known GenesFURIN
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15195437
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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