A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5630141



Internal ID21578446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:133213929..133213929hg38UCSC Ensembl
chr8:134226172..134226172hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17143144
SamplesHG00731
Known GenesWISP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5630141
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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