A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868673



Internal ID22643608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29032633..29038266hg38UCSC Ensembl
chr16:29043954..29049587hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg385634
hg195634
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17477740
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868673
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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