A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14406341



Internal ID22319086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32664906..32665310hg38UCSC Ensembl
chr19:33155812..33156216hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38405
hg19405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3222409
Supporting Variants
SamplesNA19240
Known GenesANKRD27
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14406341
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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