A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5429652



Internal ID208493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95930300..95930351hg38UCSC Ensembl
chr12:96324078..96324129hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17690075
Samples
Known GenesCCDC38
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5429652
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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