A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15204284



Internal ID21343086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:119168600..119168600hg38UCSC Ensembl
chr9:121930878..121930878hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3953644
Supporting Variants
SamplesHG002
Known GenesBRINP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15204284
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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