A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3558296



Internal ID22427099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:173737825..173738410hg38UCSC Ensembl
chr2:174602553..174603138hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38586
hg19586
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14295609, nssv14295610, nssv14295611
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3558296
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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