A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466513



Internal ID21124066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:69186313..69192026hg38UCSC Ensembl
chr12:69580093..69585806hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg385714
hg195714
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18002488
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466513
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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