A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578728



Internal ID20951799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43198150..43199408hg38UCSC Ensembl
chr17:41350167..41351425hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg381259
hg191259
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242279
Samples
Known GenesNBR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578728
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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