A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5544037



Internal ID318230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169977231..169977231hg38UCSC Ensembl
chr3:169695019..169695019hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16942461
Samples
Known GenesSEC62
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5544037
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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