A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4389432



Internal ID21380567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:220817517..220817580hg38UCSC Ensembl
chr1:220990859..220990922hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15704849
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4389432
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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