A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5431755



Internal ID210523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38118088..38118239hg38UCSC Ensembl
chr1:38583760..38583911hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16903780
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5431755
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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