A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3176548



Internal ID22333936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174320510..174323126hg38UCSC Ensembl
chr4:175241661..175244277hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg382617
hg192617
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6963n152
Supporting Variantsnssv14398907
SamplesNA19240
Known GenesCEP44
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3176548
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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