A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4391145



Internal ID21382175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37395503..37395611hg38UCSC Ensembl
chr4:37397125..37397233hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15703053
Samples
Known GenesKIAA1239
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4391145
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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