A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15189728



Internal ID21328571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45890269..45890269hg38UCSC Ensembl
chr3:45931761..45931761hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3949089
Supporting Variants
SamplesHG002
Known GenesCCR9, LZTFL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15189728
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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