A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897868



Internal ID22672977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:66006303..66012511hg38UCSC Ensembl
chr4:66872021..66878229hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg386209
hg196209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17420686
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897868
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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