A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555763



Internal ID328913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14194620..14194662hg38UCSC Ensembl
chr3:14236120..14236162hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38471
hg19471
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16930135
Samples
Known GenesLSM3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555763
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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