A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5537157



Internal ID312498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15103228..15103246hg38UCSC Ensembl
chr6:15103459..15103477hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16979061
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5537157
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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