A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837405



Internal ID22612340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:142773802..142775301hg38UCSC Ensembl
chr4:143694955..143696454hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17490248, nssv17490247
Samples
Known GenesINPP4B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837405
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