A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407679



Internal ID21065232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:18193211..18196679hg38UCSC Ensembl
chr6:18193442..18196910hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg383469
hg193469
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143045
Samples
Known GenesKDM1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407679
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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