A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638043



Internal ID21586348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71302519..71302519hg38UCSC Ensembl
chr10:73062276..73062276hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071825
SamplesNA19238
Known GenesUNC5B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638043
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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