A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4392784



Internal ID21383814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169638023..169638349hg38UCSC Ensembl
chr6:170038119..170038445hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15704007
Samples
Known GenesWDR27
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4392784
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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