A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881888



Internal ID22656864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:72791738..72805117hg38UCSC Ensembl
chr16:72825637..72839016hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg3813380
hg1913380
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17472775
Samples
Known GenesZFHX3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881888
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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