A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3184101



Internal ID22337962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:238783506..238783574hg38UCSC Ensembl
chr2:239692147..239692215hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14456052
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3184101
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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