A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13679037



Internal ID21200898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:44954010..44954010hg38UCSC Ensembl
chr13:45528145..45528145hg19UCSC Ensembl
Cytoband13q14.12
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2793567
Supporting Variants
Samples
Known GenesNUFIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13679037
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.03125


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