A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559751



Internal ID20932822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135598975..135599520hg38UCSC Ensembl
chr9:138490821..138491366hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38546
hg19546
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280148
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559751
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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