A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872606



Internal ID22647546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:48648531..48658437hg38UCSC Ensembl
chr16:48682442..48692348hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg389907
hg199907
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471571
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872606
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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