A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610150



Internal ID21558455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53674800..53674800hg38UCSC Ensembl
chr4:54540967..54540967hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38910
hg19910
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17133210
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610150
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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