A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5427090



Internal ID206001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109206267..109216003hg38UCSC Ensembl
chr1:109748889..109758625hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg389737
hg199737
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16908850
Samples
Known GenesKIAA1324, SARS
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5427090
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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