A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17150557



Internal ID21444624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:35271354..35271354hg38UCSC Ensembl
chr8:35128872..35128872hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5637521
Supporting Variants
SamplesHG00732
Known GenesUNC5D
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17150557
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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