A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16270251



Internal ID20479469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:76961658..76961658hg38UCSC Ensembl
chr13:77535793..77535793hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4761918
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16270251
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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