A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851670



Internal ID22626605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98622891..98624145hg38UCSC Ensembl
chr12:99016669..99017923hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg381255
hg191255
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467823
Samples
Known GenesIKBIP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851670
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