A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837767



Internal ID22612702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155839595..155845790hg38UCSC Ensembl
chr4:156760747..156766942hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg386196
hg196196
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493535
Samples
Known GenesASIC5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837767
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