A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17477742



Internal ID22535643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29168135..29171129hg38UCSC Ensembl
chr16:29179456..29182450hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg382995
hg192995
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5876436
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17477742
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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