A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5953332



Internal ID22728621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:159843000..159843000hg38UCSC Ensembl
chr3:159560789..159560789hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38256
hg19256
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427614
Samples
Known GenesIQCJ-SCHIP1, SCHIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5953332
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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