A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5400581



Internal ID179962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14755498..14755535hg38UCSC Ensembl
chr6:14755729..14755766hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16979157
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5400581
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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