A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5566580



Internal ID21514908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:93664715..93664784hg38UCSC Ensembl
chr6:94374433..94374502hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17153962
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5566580
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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