A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5643072



Internal ID21591377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158701175..158701175hg38UCSC Ensembl
chr6:159122207..159122207hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg381141
hg191141
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17150968, nssv17151920
SamplesHG00512, NA19239
Known GenesSYTL3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5643072
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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