A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638894



Internal ID21587199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129886017..129886017hg38UCSC Ensembl
chr7:129525857..129525857hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg38669
hg19669
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17157229
SamplesNA18534
Known GenesUBE2H
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638894
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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