A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5949210



Internal ID22724661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38380304..38387096hg38UCSC Ensembl
chr22:38776309..38783101hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg386793
hg196793
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17391854
Samples
Known GenesLOC400927
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5949210
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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