A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17580779



Internal ID21772822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126661206..126661278hg38UCSC Ensembl
chr9:129423485..129423557hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6020381
Supporting Variants
Samples
Known GenesLMX1B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17580779
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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