A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4392243



Internal ID21383273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:8432263..8434992hg38UCSC Ensembl
chr6:8432496..8435225hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg382730
hg192730
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15703695
Samples
Known GenesSLC35B3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4392243
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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