A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5838934



Internal ID22613869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:31282229..31300187hg38UCSC Ensembl
chr4:31283851..31301809hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3817959
hg1917959
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493471
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5838934
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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