A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14405742



Internal ID22290316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25686249..25687234hg38UCSC Ensembl
chr15:25931396..25932381hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38986
hg19986
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3204140
Supporting Variants
SamplesNA19240
Known GenesATP10A
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14405742
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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