A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399096



Internal ID21056649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:44839853..44849392hg38UCSC Ensembl
chr6:44807590..44817129hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg389540
hg199540
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18144098
Samples
Known GenesSUPT3H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399096
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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