A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4390588



Internal ID21381723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:96777448..96778241hg38UCSC Ensembl
chr3:96496292..96497085hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38794
hg19794
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15707167
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4390588
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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