A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5552953



Internal ID326251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23580163..23580204hg38UCSC Ensembl
chr10:23869092..23869133hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17033770
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5552953
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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