A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17158405



Internal ID21426928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20278025..20278088hg38UCSC Ensembl
chr7:20317648..20317711hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5571439
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17158405
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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