A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18060969



Internal ID20628009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:33341157..33343566hg38UCSC Ensembl
chr1:33806758..33809167hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg382410
hg192410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6335341
Supporting Variants
Samples
Known GenesPHC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18060969
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