A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5574632



Internal ID21523049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:35487191..35487247hg38UCSC Ensembl
chr8:35344709..35344765hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17156149
SamplesNA24385
Known GenesUNC5D
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5574632
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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