A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5609625



Internal ID21557930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:147159768..147159768hg38UCSC Ensembl
chr4:148080920..148080920hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17139517
SamplesHG02492
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5609625
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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