A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17154283



Internal ID21413137
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 StatusS
Merged Variantsnsv5582315
Supporting Variants
SamplesHG00513
Known GenesEYA4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17154283
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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