A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4389227



Internal ID21380362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:115298550..115298812hg38UCSC Ensembl
chr1:115841171..115841433hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38263
hg19263
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15703682
Samples
Known GenesNGF
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4389227
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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