A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760236



Internal ID20536096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77332329..77332329hg38UCSC Ensembl
chr11:77043374..77043374hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291155
Samples
Known GenesPAK1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760236
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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