A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5654023



Internal ID21602328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78194138..78194138hg38UCSC Ensembl
chr11:77905184..77905184hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17076776
SamplesHG02011
Known GenesUSP35
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5654023
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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