A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011301



Internal ID21920644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124670436..124670524hg38UCSC Ensembl
chr9:127432715..127432803hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590281
Samples
Known GenesMIR181A2HG, NR6A1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011301
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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