A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3182968



Internal ID22337377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:31430754..31433157hg38UCSC Ensembl
chr1:31903601..31906004hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg382404
hg192404
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv174n152
Supporting Variantsnssv14393298, nssv14393297
SamplesNA19240
Known GenesSERINC2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3182968
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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