A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14445638



Internal ID22225710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25871685..25871685hg38UCSC Ensembl
chr15:26116832..26116832hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3543586
Supporting Variants
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14445638
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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