A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985727



Internal ID20552767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95210776..95211153hg38UCSC Ensembl
chr10:96970533..96970910hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38378
hg19378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439769
Supporting Variants
Samples
Known GenesC10orf129
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985727
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00109


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