A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13693814



Internal ID21215662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43128238..43128238hg38UCSC Ensembl
chr17:41280255..41280255hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2797774
Supporting Variants
Samples
Known GenesNBR2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13693814
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.359375


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