A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5652626



Internal ID21600931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:82995272..82995272hg38UCSC Ensembl
chr11:82706314..82706314hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17076269
SamplesHG02818
Known GenesRAB30
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5652626
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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