A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578408



Internal ID20951479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:29237784..29238167hg38UCSC Ensembl
chr17:27564802..27565185hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38384
hg19384
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241659
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578408
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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