A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5565324



Internal ID21513636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:61432828..61434877hg38UCSC Ensembl
chr6:61904144..61906194hg19UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg382050
hg192051
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17141350
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5565324
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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