A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405492



Internal ID21063045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13847001..13856700hg38UCSC Ensembl
chr6:13847232..13856931hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg389700
hg199700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138389
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405492
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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