A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17131263



Internal ID21445549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38807771..38807951hg38UCSC Ensembl
chr4:38809392..38809572hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5568509
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17131263
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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