A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18057679



Internal ID20624719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:223690646..223691829hg38UCSC Ensembl
chr1:223878348..223879531hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg381184
hg191184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6327454
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18057679
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