A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194256



Internal ID20761296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24510320..24608839hg38UCSC Ensembl
chr10:24799249..24897768hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3898520
hg1998520
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6451582
Supporting Variants
Samples
Known GenesARHGAP21, KIAA1217
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194256
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