A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15191004



Internal ID21329863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149706417..149706417hg38UCSC Ensembl
chr3:149424204..149424204hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3945794
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15191004
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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