A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15188827



Internal ID21327669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3790628..3790628hg38UCSC Ensembl
chr3:3832312..3832312hg19UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3935591
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15188827
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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