A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv174n152



Internal ID22815877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:31430754..31434139hg38UCSC Ensembl
chr1:31903601..31906986hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg383386
hg193386
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3182968, nsv3178252
SamplesNA19240, HG00733
Known GenesSERINC2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv174n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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