A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888997



Internal ID22664008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:182714566..182714802hg38UCSC Ensembl
chr3:182432354..182432590hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38237
hg19237
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416221
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888997
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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