A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17854581



Internal ID22038224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:108388680..108388680hg38UCSC Ensembl
chr4:109309836..109309836hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6255124
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17854581
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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