A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5643427



Internal ID21591732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:61282240..61282240hg38UCSC Ensembl
chr5:60578067..60578067hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg382557
hg192557
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17156084
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5643427
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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