A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5883790



Internal ID22658772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23458984..23472200hg38UCSC Ensembl
chr16:23470305..23483521hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3813217
hg1913217
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17477672
Samples
Known GenesGGA2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5883790
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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