A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15193038



Internal ID21331920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99427145..99427145hg38UCSC Ensembl
chr13:100079399..100079399hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38226
hg19226
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3928440
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15193038
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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