A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594534



Internal ID20967605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:17277478..17278136hg38UCSC Ensembl
chr17:17180792..17181450hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38659
hg19659
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242080
Samples
Known GenesCOPS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594534
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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