A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2809563



Internal ID21254901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:54169925..54169925hg38UCSC Ensembl
chr4:55036092..55036092hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg381428
hg191428
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13711227
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2809563
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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