A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027247



Internal ID21936590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:112071607..112071768hg38UCSC Ensembl
chr11:111942331..111942492hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600393
Samples
Known GenesPIH1D2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027247
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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