A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486284



Internal ID21143837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:127825497..127825906hg38UCSC Ensembl
chr12:128310042..128310451hg19UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg38410
hg19410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17997505
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486284
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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