A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892199



Internal ID22667245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:159800641..159800943hg38UCSC Ensembl
chr3:159518430..159518732hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17410211
Samples
Known GenesIQCJ-SCHIP1, SCHIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892199
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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