A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5577533



Internal ID21525987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42664096..42664190hg38UCSC Ensembl
chr6:42631834..42631928hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17152021
SamplesHG03125
Known GenesUBR2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5577533
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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