A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14398295



Internal ID22311820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196317470..196317580hg38UCSC Ensembl
chr3:196044341..196044451hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3188147
Supporting Variants
SamplesNA19240
Known GenesTCTEX1D2, TM4SF19-TCTEX1D2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14398295
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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