A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470138



Internal ID21127691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:45942401..45944300hg38UCSC Ensembl
chr12:46336184..46338083hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18000434
Samples
Known GenesSCAF11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470138
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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