A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5640590



Internal ID21588895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71296862..71296862hg38UCSC Ensembl
chr10:73056619..73056619hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071823
SamplesNA19239
Known GenesUNC5B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5640590
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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