A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17477743



Internal ID22535644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29224275..29226245hg38UCSC Ensembl
chr16:29235596..29237566hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381971
hg191971
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5879161
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17477743
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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