A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6244487



Internal ID22049097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:85857759..85857759hg38UCSC Ensembl
chr5:85153577..85153577hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17855631
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6244487
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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