A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5573022



Internal ID21521419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:51203205..51203474hg38UCSC Ensembl
chr7:51270902..51271171hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17156422
SamplesNA19239
Known GenesCOBL
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5573022
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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