A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4391394



Internal ID21382424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74798955..74799032hg38UCSC Ensembl
chr15:75091296..75091373hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15705940
Samples
Known GenesCSK
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4391394
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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