A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887385



Internal ID22662377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74791005..74808206hg38UCSC Ensembl
chr16:74824903..74842104hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3817202
hg1917202
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473364
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887385
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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