A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5614833



Internal ID21563138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38530451..38530451hg38UCSC Ensembl
chr1:38996123..38996123hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17065042
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5614833
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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