A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17088097



Internal ID21459641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:30391737..30391737hg38UCSC Ensembl
chr13:30965874..30965874hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg382203
hg192203
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5653311
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17088097
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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