A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18064450



Internal ID20631490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:81706601..81712300hg38UCSC Ensembl
chr1:82172286..82177985hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg385700
hg195700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6322522
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18064450
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


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