A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17370570



Internal ID22596239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1738369..1739167hg38UCSC Ensembl
chr16:1788370..1789168hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38799
hg19799
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5939172
Supporting Variants
Samples
Known GenesMAPK8IP3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17370570
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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