A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15199446



Internal ID21338242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:4346658..4346969hg38UCSC Ensembl
chr9:4346658..4346969hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3926000
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15199446
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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