A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5557844



Internal ID330928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157365773..157365824hg38UCSC Ensembl
chr6:157786805..157786856hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38748
hg19748
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16989834
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5557844
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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