A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17065976



Internal ID21486956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:47686733..47686733hg38UCSC Ensembl
chr1:48152405..48152405hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5622460
Supporting Variants
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17065976
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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