A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14459668



Internal ID22212217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:37940975..37941409hg38UCSC Ensembl
chr9:37940972..37941406hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38435
hg19435
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3195365
Supporting Variants
SamplesHG00733
Known GenesSHB
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14459668
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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