A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3190713



Internal ID22341540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63125594..63125829hg38UCSC Ensembl
chr15:63417793..63418028hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38236
hg19236
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14444560
SamplesHG00733
Known GenesLACTB
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3190713
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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