A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16273863



Internal ID20483081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19068329..19068448hg38UCSC Ensembl
chr9:19068327..19068446hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4748073
Supporting Variants
Samples
Known GenesHAUS6
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16273863
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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