A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16274122



Internal ID20483340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34904795..34904795hg38UCSC Ensembl
chr9:34904792..34904792hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4751949
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16274122
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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