A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555870



Internal ID329019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:3155635..3155686hg38UCSC Ensembl
chr2:3159406..3159457hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16900950
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555870
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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