A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3183128



Internal ID22337457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202203766..202206416hg38UCSC Ensembl
chr1:202172894..202175544hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg382651
hg192651
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv528n152
Supporting Variantsnssv14461978, nssv14465163
SamplesHG00733
Known GenesLGR6
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3183128
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