A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462288



Internal ID21119841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:1652246..1656165hg38UCSC Ensembl
chr12:1761412..1765331hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg383920
hg193920
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17998091
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462288
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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