A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2811655



Internal ID21256994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2099223..2099223hg38UCSC Ensembl
chr5:2099337..2099337hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13700552
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2811655
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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