A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5433311



Internal ID212033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37399693..37427840hg38UCSC Ensembl
chr1:37865294..37893441hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3828148
hg1928148
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16903764
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5433311
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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