A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6066614



Internal ID21975847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:92683190..92683190hg38UCSC Ensembl
chr7:92312504..92312504hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17569046
Samples
Known GenesCDK6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6066614
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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