A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052494



Internal ID20619534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161107968..161110204hg38UCSC Ensembl
chr1:161077758..161079994hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg382237
hg192237
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6318688
Supporting Variants
Samples
Known GenesPFDN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052494
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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