A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5959943



Internal ID22734962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32472836..32472836hg38UCSC Ensembl
chr7:32512448..32512448hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446541
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5959943
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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