A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6061453



Internal ID21970686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:148209954..148209954hg38UCSC Ensembl
chr5:147589517..147589517hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17567782
Samples
Known GenesSPINK6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6061453
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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