A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5461833



Internal ID239776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:82918894..82956691hg38UCSC Ensembl
chr5:82214713..82252510hg19UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg3837798
hg1937798
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16968650
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5461833
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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