A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5966327



Internal ID22741262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:156387014..156387014hg38UCSC Ensembl
chr3:156104803..156104803hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17422926
Samples
Known GenesKCNAB1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5966327
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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