A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413581



Internal ID21071134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:18161462..18163076hg38UCSC Ensembl
chr6:18161693..18163307hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg381615
hg191615
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143304
Samples
Known GenesKDM1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413581
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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