A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6260524



Internal ID22065134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77908945..77908945hg38UCSC Ensembl
chr5:77204769..77204769hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17858133
Samples
Known GenesLOC101929154
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6260524
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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