A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052082



Internal ID20619122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155566903..155568339hg38UCSC Ensembl
chr1:155536694..155538130hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg381437
hg191437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321561
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052082
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