A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16270566



Internal ID20479784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74346506..74346506hg38UCSC Ensembl
chr9:76961422..76961422hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4767525
Supporting Variants
Samples
Known GenesMIR6130
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16270566
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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