A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18174072



Internal ID20741112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129611566..129612496hg38UCSC Ensembl
chr9:132373845..132374775hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38931
hg19931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6444751
Supporting Variants
Samples
Known GenesC9orf50, NTMT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18174072
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00317


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