A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473394



Internal ID21130947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:12842565..12846054hg38UCSC Ensembl
chr12:12995499..12998988hg19UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg383490
hg193490
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17997532
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473394
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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