A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5551013



Internal ID324504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:17157102..17157137hg38UCSC Ensembl
chr12:17310036..17310071hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17054439
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5551013
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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