A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17855386



Internal ID22039029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:22332581..22332581hg38UCSC Ensembl
chr4:22334204..22334204hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6243846
Supporting Variants
Samples
Known GenesLOC100505912
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17855386
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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