A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5959721



Internal ID22734743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:49860838..49865071hg38UCSC Ensembl
chr22:50254486..50258719hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg384234
hg194234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17407824
Samples
Known GenesZBED4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5959721
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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