A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886664



Internal ID22661653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30323366..30327349hg38UCSC Ensembl
chr16:30334687..30338670hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg383984
hg193984
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17478291
Samples
Known GenesLOC595101
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886664
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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