A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3192017



Internal ID22342654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:72685369..72685494hg38UCSC Ensembl
chr17:70681508..70681633hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14446583
SamplesHG00733
Known GenesSLC39A11
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3192017
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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