A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562661



Internal ID335607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:156502687..156502738hg38UCSC Ensembl
chr6:156823821..156823872hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg386007
hg196007
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16989135
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562661
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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