A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6255597



Internal ID22060207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:160003993..160003993hg38UCSC Ensembl
chr4:160925145..160925145hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38224
hg19224
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17856274
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6255597
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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