A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089632



Internal ID21998865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64759013..64759013hg38UCSC Ensembl
chr11:64526485..64526485hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583513
Samples
Known GenesPYGM
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089632
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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