A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2811031



Internal ID21256369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99589061..99589061hg38UCSC Ensembl
chr4:100510218..100510218hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38628
hg19628
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13708236
Samples
Known GenesMTTP
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2811031
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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