A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5619618



Internal ID21567923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158473767..158473767hg38UCSC Ensembl
chr1:158443557..158443557hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17061220, nssv17061221, nssv17061219
SamplesHG03125, NA19650, HG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5619618
Frequency
Sample Size35
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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