A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5540136



Internal ID314947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3626836..3626836hg38UCSC Ensembl
chr6:3627070..3627070hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16978039
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5540136
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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