A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14453538



Internal ID22217710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25756994..25759805hg38UCSC Ensembl
chr15:26002141..26004952hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg382812
hg192812
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3200309
Supporting Variants
SamplesHG00733
Known GenesATP10A
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14453538
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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