A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15195536



Internal ID21334445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10884128..10884128hg38UCSC Ensembl
chr16:10977985..10977985hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg381005
hg191005
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3926908
Supporting Variants
SamplesHG002
Known GenesCIITA
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15195536
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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