A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209615



Internal ID20776655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:138053724..138084338hg38UCSC Ensembl
chr3:137772566..137803180hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3830615
hg1930615
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6364073
Supporting Variants
Samples
Known GenesDZIP1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209615
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00018


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