A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17590277



Internal ID21782320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112316979..112317600hg38UCSC Ensembl
chr9:115079259..115079880hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38622
hg19622
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6002650
Supporting Variants
Samples
Known GenesMIR3134, PTBP3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17590277
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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