A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5439011



Internal ID217559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:135225218..135242379hg38UCSC Ensembl
chr2:135982788..135999949hg19UCSC Ensembl
Cytoband2q21.3
Allele length
AssemblyAllele length
hg3817162
hg1917162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16918820
Samples
Known GenesZRANB3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5439011
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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