A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5424136



Internal ID203136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9810682..9813072hg38UCSC Ensembl
chr1:9870740..9873130hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg382391
hg192391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16891282
Samples
Known GenesCLSTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5424136
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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