A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5431505



Internal ID210279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26460535..26460731hg38UCSC Ensembl
chr1:26787026..26787222hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16902465
Samples
Known GenesDHDDS
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5431505
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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