A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5554807



Internal ID327980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:1376975..1377026hg38UCSC Ensembl
chr2:1380747..1380798hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg386018
hg196018
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16898963
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5554807
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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