A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17372536



Internal ID22598205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1542248..1543075hg38UCSC Ensembl
chr16:1592249..1593076hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38828
hg19828
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5944921
Supporting Variants
Samples
Known GenesIFT140, TMEM204
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17372536
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