A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3183123



Internal ID22337454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75610972..75611059hg38UCSC Ensembl
chr6:76320688..76320775hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14457353
SamplesHG00733
Known GenesSENP6
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3183123
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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