A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5631824



Internal ID21580129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71223761..71223761hg38UCSC Ensembl
chr10:72983518..72983518hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071817
SamplesHG00096
Known GenesUNC5B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5631824
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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