A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4392691



Internal ID21383721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:148272929..148274761hg38UCSC Ensembl
chr6:148594065..148595897hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg381833
hg191833
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15703958
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4392691
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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