A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903446



Internal ID22678614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43186570..43186766hg38UCSC Ensembl
chr6:43154308..43154504hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17438996
Samples
Known GenesCUL9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903446
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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