A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458905



Internal ID21116458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:66358467..66362123hg38UCSC Ensembl
chr12:66752247..66755903hg19UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg383657
hg193657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18003055
Samples
Known GenesGRIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458905
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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