A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17150488



Internal ID21485227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:21851442..21851620hg38UCSC Ensembl
chr6:21851673..21851851hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5581908
Supporting Variants
SamplesNA12878
Known GenesCASC15
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17150488
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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