A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14439300



Internal ID22236074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137145034..137145091hg38UCSC Ensembl
chr9:140039486..140039543hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3200020
Supporting Variants
SamplesHG00733
Known GenesGRIN1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14439300
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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