A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199028



Internal ID20766068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7617680..7657473hg38UCSC Ensembl
chr19:7682566..7722359hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3839794
hg1939794
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6520929
Supporting Variants
Samples
Known GenesCAMSAP3, PCP2, PET100, STXBP2, XAB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199028
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