A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5580108



Internal ID21528594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:16266086..16266160hg38UCSC Ensembl
chr6:16266317..16266391hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17156801
SamplesHG00512
Known GenesGMPR
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5580108
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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