A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5582315



Internal ID21530826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:133502724..133502803hg38UCSC Ensembl
chr6:133823862..133823941hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17154283
SamplesHG00513
Known GenesEYA4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5582315
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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