A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2811408



Internal ID21256746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:55897016..55897016hg38UCSC Ensembl
chr5:55192844..55192844hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13700624
Samples
Known GenesIL31RA
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2811408
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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