A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201464



Internal ID20768504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:53288901..53385619hg38UCSC Ensembl
chr1:53754573..53851291hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3896719
hg1996719
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6324218
Supporting Variants
Samples
Known GenesLRP8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201464
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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