A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401188



Internal ID21058741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:18218412..18219149hg38UCSC Ensembl
chr6:18218643..18219380hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38738
hg19738
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143047
Samples
Known GenesKDM1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401188
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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