A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5840024



Internal ID22614959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:66006301..66012617hg38UCSC Ensembl
chr4:66872019..66878335hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg386317
hg196317
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17490460
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5840024
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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