A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6260357



Internal ID22064967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:57401345..57401345hg38UCSC Ensembl
chr5:56697172..56697172hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17858506
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6260357
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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