A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398364



Internal ID21055917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:17734363..18292190hg38UCSC Ensembl
chr6:17734594..18292421hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38557828
hg19557828
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143281
Samples
Known GenesDEK, KDM1B, KIF13A, NHLRC1, TPMT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398364
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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