A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5906399



Internal ID22681599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:159711196..159711394hg38UCSC Ensembl
chr3:159428985..159429183hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38199
hg19199
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428751
Samples
Known GenesIQCJ-SCHIP1, SCHIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5906399
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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