A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5436592



Internal ID215205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:136059127..136059208hg38UCSC Ensembl
chr2:136816697..136816778hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16918880
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5436592
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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