A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16278051



Internal ID20487269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:100100580..100100580hg38UCSC Ensembl
chr9:102862862..102862862hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38540
hg19540
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4767653
Supporting Variants
Samples
Known GenesINVS
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16278051
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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