A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000760



Internal ID21910103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128129949..128130316hg38UCSC Ensembl
chr9:130892228..130892595hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38368
hg19368
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596033
Samples
Known GenesPTGES2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000760
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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