A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5672306



Internal ID21620611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:30750657..30797503hg38UCSC Ensembl
chr17:29077675..29124521hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3846847
hg1946847
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17086826
Samples
Known GenesCRLF3, SUZ12P1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5672306
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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