A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14382397



Internal ID22287922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:871743..872329hg38UCSC Ensembl
chr9:871743..872329hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38587
hg19587
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3204811
Supporting Variants
SamplesNA19240
Known GenesDMRT1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14382397
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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