A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4731013



Internal ID20506931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74126930..74126982hg38UCSC Ensembl
chr9:76741846..76741898hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16280616
Samples
Known GenesMIR6130
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4731013
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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