A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6255955



Internal ID22060565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:9796721..9796721hg38UCSC Ensembl
chr5:9796833..9796833hg19UCSC Ensembl
Cytoband5p15.31
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 Variantsnssv17857147
Samples
Known GenesLOC285692
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6255955
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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