A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876337



Internal ID22651297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:49296462..49300161hg38UCSC Ensembl
chr16:49330373..49334072hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg383700
hg193700
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17478997
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876337
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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