A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403798



Internal ID21061351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24650142..24650791hg38UCSC Ensembl
chr6:24650370..24651019hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38650
hg19650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140665
Samples
Known GenesTDP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403798
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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