A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5578000



Internal ID21526461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151450407..151450485hg38UCSC Ensembl
chr6:151771542..151771620hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17148415
SamplesHG00732
Known GenesRMND1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5578000
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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