A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5619063



Internal ID21567368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:95400531..95400531hg38UCSC Ensembl
chr4:96321682..96321682hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17127062
SamplesHG03486
Known GenesUNC5C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5619063
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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