A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5598073



Internal ID21546694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:39217033..39217087hg38UCSC Ensembl
chr21:40588959..40589013hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17118584
SamplesHG00731
Known GenesBRWD1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5598073
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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