A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5642297



Internal ID21590602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:142860704..142860704hg38UCSC Ensembl
chr5:142240269..142240269hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38996
hg19996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17119923
SamplesHG02492
Known GenesARHGAP26, ARHGAP26-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5642297
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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