A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18058899



Internal ID20625939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:235991532..235994542hg38UCSC Ensembl
chr1:236154832..236157842hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg383011
hg193011
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6323640
Supporting Variants
Samples
Known GenesNID1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18058899
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