A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5574417



Internal ID21522832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31455358..31455565hg38UCSC Ensembl
chr6:31423135..31423342hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg38208
hg19208
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17144049
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5574417
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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