A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060584



Internal ID21969817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:31292824..31292824hg38UCSC Ensembl
chr5:31292931..31292931hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17555882
Samples
Known GenesCDH6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060584
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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