A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002650



Internal ID21911993
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 StatusM
Merged Variants
Supporting Variantsnssv17590277
Samples
Known GenesMIR3134, PTBP3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002650
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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