A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012010



Internal ID21921353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132270121..132270202hg38UCSC Ensembl
chr9:135145508..135145589hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580269
Samples
Known GenesSETX
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012010
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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