A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895433



Internal ID22670515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:182847543..182847700hg38UCSC Ensembl
chr3:182565331..182565488hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412924
Samples
Known GenesATP11B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895433
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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