A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5838930



Internal ID22613865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:29527580..29531633hg38UCSC Ensembl
chr4:29529202..29533255hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg384054
hg194054
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493450
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5838930
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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