A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413281



Internal ID21070834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36511760..36529416hg38UCSC Ensembl
chr6:36479537..36497193hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3817657
hg1917657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141758
Samples
Known GenesSTK38
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413281
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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