A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178491



Internal ID20745531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:34692394..34919305hg38UCSC Ensembl
chr10:34981322..35208233hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38226912
hg19226912
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6451980
Supporting Variants
Samples
Known GenesPARD3, PARD3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178491
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