A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4389005



Internal ID21380140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33575772..33576080hg38UCSC Ensembl
chr9:33575770..33576078hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12n171
Supporting Variantsnssv15704631
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4389005
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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