A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5659012



Internal ID21607317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:88506963..88506963hg38UCSC Ensembl
chr11:88240131..88240131hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17076581
SamplesHG03486
Known GenesGRM5, GRM5-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5659012
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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