A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587290



Internal ID20960361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:18060101..18060786hg38UCSC Ensembl
chr17:17963415..17964100hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38686
hg19686
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242099
Samples
Known GenesGID4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587290
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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