A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881707



Internal ID22656683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:31278413..31279657hg38UCSC Ensembl
chr16:31289734..31290978hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381245
hg191245
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17478305
Samples
Known GenesITGAM
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881707
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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