A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592669



Internal ID20965740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6322003..6322842hg38UCSC Ensembl
chr17:6225323..6226162hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38840
hg19840
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242611
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592669
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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