A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180465



Internal ID20747505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25625138..25625667hg38UCSC Ensembl
chr10:25914067..25914596hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38530
hg19530
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452572
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180465
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00047


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