A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18175697



Internal ID20742737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15925337..15926193hg38UCSC Ensembl
chr9:15925335..15926191hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38857
hg19857
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6419118
Supporting Variants
Samples
Known GenesCCDC171
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18175697
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00011


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