A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5569402



Internal ID21517759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:42021918..42022101hg38UCSC Ensembl
chr4:42023935..42024118hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17132447
SamplesHG00731
Known GenesSLC30A9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5569402
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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