A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5952034



Internal ID22727369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44572849..44572849hg38UCSC Ensembl
chr3:44614341..44614341hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38202
hg19202
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428932
Samples
Known GenesZKSCAN7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5952034
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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