A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17076206



Internal ID21481675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77332351..77332351hg38UCSC Ensembl
chr11:77043396..77043396hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5645307
Supporting Variants
SamplesHG03683
Known GenesPAK1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17076206
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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