A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16962826



Internal ID42541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16098767..16098767hg38UCSC Ensembl
chr5:16098876..16098876hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5536107
Supporting Variants
Samples
Known GenesMARCH11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16962826
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.016373


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