A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17064593



Internal ID21502408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:31176667..31176667hg38UCSC Ensembl
chr1:31649514..31649514hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5612362
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17064593
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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