A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5572250



Internal ID21520637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:34528514..34528637hg38UCSC Ensembl
chr8:34386032..34386155hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17158585
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5572250
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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