A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3179123



Internal ID22335377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155309422..155313019hg38UCSC Ensembl
chr3:155027211..155030808hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg383598
hg193598
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6212n152
Supporting Variantsnssv14397095
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3179123
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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