A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4390979



Internal ID21382113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:50303776..50305719hg38UCSC Ensembl
chr1:50769448..50771391hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg381944
hg191944
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15706860
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4390979
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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