A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5838502



Internal ID22613437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:185443931..185445569hg38UCSC Ensembl
chr4:186365085..186366723hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg381639
hg191639
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493698
Samples
Known GenesC4orf47, CCDC110
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5838502
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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