A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15204280



Internal ID21343082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87818955..87818955hg38UCSC Ensembl
chr9:90433870..90433870hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3953959
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15204280
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