A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5964356



Internal ID22739291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45890270..45890270hg38UCSC Ensembl
chr3:45931762..45931762hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17422514
Samples
Known GenesCCR9, LZTFL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5964356
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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