A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17137804



Internal ID21477795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45890308..45890308hg38UCSC Ensembl
chr3:45931800..45931800hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5609633
Supporting Variants
SamplesHG03486
Known GenesCCR9, LZTFL1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17137804
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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