A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5838963



Internal ID22613898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:36404167..36409291hg38UCSC Ensembl
chr4:36405789..36410913hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg385125
hg195125
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17494468
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5838963
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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