A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14431136



Internal ID22173570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105741497..106745274hg38UCSC Ensembl
chr14:106207834..107174928hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg381003778
hg19967095
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3228877
Supporting Variants
SamplesHG00514
Known GenesADAM6, KIAA0125, LINC00221, LINC00226
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14431136
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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