A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5461151



Internal ID239111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159927300..160654790hg38UCSC Ensembl
chr6:160348332..161075822hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38727491
hg19727491
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16989224
Samples
Known GenesAIRN, IGF2R, LOC729603, LPA, LPAL2, SLC22A1, SLC22A2, SLC22A3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5461151
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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