A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15190493



Internal ID21329347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184713008..184713008hg38UCSC Ensembl
chr3:184430796..184430796hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3945221
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15190493
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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