A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236632



Internal ID20803672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:45464575..45465873hg38UCSC Ensembl
chr7:45504174..45505472hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg381299
hg191299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6602039
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236632
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00016


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