A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5605927



Internal ID21554232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23710865..23710865hg38UCSC Ensembl
chr1:24037355..24037355hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17063327, nssv17063328
SamplesHG03125, HG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5605927
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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