A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15746482



Internal ID21391320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133291853..133292569hg38UCSC Ensembl
chr10:135105357..135106073hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38717
hg19717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4431269
Supporting Variants
SamplesNB12
Known GenesTUBGCP2
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15746482
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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