A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16262311



Internal ID20471529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77451587..77451909hg38UCSC Ensembl
chr11:77162632..77162954hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4748638
Supporting Variants
Samples
Known GenesPAK1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16262311
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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