A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17583170



Internal ID21775213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137838186..137840451hg38UCSC Ensembl
chr9:140732638..140734903hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg382266
hg192266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6005088
Supporting Variants
Samples
Known GenesMIR602
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17583170
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