A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4388955



Internal ID21380090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:4628118..4629381hg38UCSC Ensembl
chr9:4628118..4629381hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg381264
hg191264
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15704575
Samples
Known GenesSPATA6L
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4388955
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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