A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5644069



Internal ID21592374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71296909..71296909hg38UCSC Ensembl
chr10:73056666..73056666hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38199
hg19199
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071824
SamplesHG00732
Known GenesUNC5B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5644069
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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