A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5537033



Internal ID252602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6590200..6590200hg38UCSC Ensembl
chr10:6632162..6632162hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17029001
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5537033
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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