A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877632



Internal ID22652596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9111031..9139857hg38UCSC Ensembl
chr16:9204888..9233714hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3828827
hg1928827
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474822
Samples
Known GenesC16orf72
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877632
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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