A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17065041



Internal ID21452226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38530166..38530166hg38UCSC Ensembl
chr1:38995838..38995838hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5623504
Supporting Variants
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17065041
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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