A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102662



Internal ID22011895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1424047..1429348hg38UCSC Ensembl
chr17:1327341..1332642hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg385302
hg195302
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622391
Samples
Known GenesCRK
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102662
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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