A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15204820



Internal ID21343623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32463889..32463889hg38UCSC Ensembl
chr9:32463887..32463887hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3950116
Supporting Variants
SamplesHG002
Known GenesDDX58
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15204820
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer