A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857611



Internal ID22632546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94660676..94679607hg38UCSC Ensembl
chr14:95127013..95145944hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3818932
hg1918932
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17470167
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857611
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer