A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5433977



Internal ID212671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:11416535..11417677hg38UCSC Ensembl
chr4:11418159..11419301hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg381143
hg191143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16946851
Samples
Known GenesHS3ST1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5433977
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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