A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593616



Internal ID20966687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:19847567..19848776hg38UCSC Ensembl
chr17:19750880..19752089hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg381210
hg191210
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241479
Samples
Known GenesULK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593616
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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