A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466903



Internal ID21124456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:8900276..8901315hg38UCSC Ensembl
chr12:9052872..9053911hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg381040
hg191040
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18004811
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466903
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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