A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5651931



Internal ID21600236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77279525..77279525hg38UCSC Ensembl
chr11:76990570..76990570hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17076205
SamplesNA24385
Known GenesGDPD4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5651931
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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