A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2811030



Internal ID21256368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99589036..99589036hg38UCSC Ensembl
chr4:100510193..100510193hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38670
hg19670
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13711093, nssv13707790
Samples
Known GenesMTTP
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2811030
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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