A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18060362



Internal ID20627402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:31097988..31098930hg38UCSC Ensembl
chr1:31570835..31571777hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg38943
hg19943
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321101
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18060362
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