A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582318



Internal ID20955389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:29364435..29364871hg38UCSC Ensembl
chr17:27691453..27691889hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38437
hg19437
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241674
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582318
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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