A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5583811



Internal ID21532341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:50798243..50798553hg38UCSC Ensembl
chr6:50765956..50766266hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17153647
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5583811
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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