A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16293172



Internal ID20502390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:30612155..30612155hg38UCSC Ensembl
chr13:31186292..31186292hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4757135
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16293172
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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