A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15193801



Internal ID21332693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78599765..78599765hg38UCSC Ensembl
chr15:78892107..78892107hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38795
hg19795
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3934046
Supporting Variants
SamplesHG002
Known GenesCHRNA3
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15193801
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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