A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17377319



Internal ID22435189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22967716..22967782hg38UCSC Ensembl
chr15:22905286..22905352hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5940779
Supporting Variants
Samples
Known GenesCYFIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17377319
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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