A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17605734



Internal ID21797781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:29835089..29835149hg38UCSC Ensembl
chr13:30409226..30409286hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6023518
Supporting Variants
Samples
Known GenesUBL3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17605734
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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