A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5402625



Internal ID181994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:64888814..64888865hg38UCSC Ensembl
chr3:64874489..64874540hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16933145
Samples
Known GenesADAMTS9-AS2, MIR548A2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5402625
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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