A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602381



Internal ID20975452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106559419..106560777hg38UCSC Ensembl
chr6:107007294..107008652hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381359
hg191359
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136868
Samples
Known GenesAIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602381
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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