A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14391693



Internal ID22290465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:138226416..138253879hg38UCSC Ensembl
chr9:141116866..141144329hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3827464
hg1927464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3227885
Supporting Variants
SamplesNA19240
Known GenesFAM157B
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14391693
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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