A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5626088



Internal ID21574393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87063659..87063659hg38UCSC Ensembl
chr10:88823416..88823416hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17072206
SamplesHG01505
Known GenesGLUD1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5626088
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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