A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17075706



Internal ID21415421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77332356..77332356hg38UCSC Ensembl
chr11:77043401..77043401hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38258
hg19258
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5658716
Supporting Variants
SamplesHG00731
Known GenesPAK1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17075706
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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