A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183981



Internal ID20751021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12393188..12415445hg38UCSC Ensembl
chr10:12435187..12457444hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3822258
hg1922258
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6446191
Supporting Variants
Samples
Known GenesCAMK1D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183981
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