A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671151



Internal ID21619456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:60037601..60109298hg38UCSC Ensembl
chr17:58114962..58186659hg19UCSC Ensembl
Cytoband17q23.1
Allele length
AssemblyAllele length
hg3871698
hg1971698
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17093467
SamplesNA19239
Known GenesHEATR6, LOC645638, LOC653653, MIR4737
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671151
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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