A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586332



Internal ID20959403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9601013..9602129hg38UCSC Ensembl
chr17:9504330..9505446hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg381117
hg191117
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243395
Samples
Known GenesWDR16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586332
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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