A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2811832



Internal ID21257170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:69377508..69377508hg38UCSC Ensembl
chr5:68673335..68673335hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13700219
Samples
Known GenesRAD17
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2811832
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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