A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870748



Internal ID22645684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81636968..81642122hg38UCSC Ensembl
chr16:81670573..81675727hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg385155
hg195155
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474023
Samples
Known GenesCMIP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870748
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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