A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5620644



Internal ID21568949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:154718176..154718176hg38UCSC Ensembl
chr4:155639328..155639328hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17135181
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5620644
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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