A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15190178



Internal ID21329025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:182153133..182153133hg38UCSC Ensembl
chr3:181870921..181870921hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3951415
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15190178
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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