A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5883847



Internal ID22658829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:72059137..72062773hg38UCSC Ensembl
chr16:72093036..72096672hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg383637
hg193637
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv847n209
Supporting Variantsnssv17472738, nssv17472739, nssv17472740
Samples
Known GenesHP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5883847
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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