A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17978105



Internal ID20545145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112142154..112144540hg38UCSC Ensembl
chr10:113901912..113904298hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg382387
hg192387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440100
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17978105
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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