A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571654



Internal ID20944725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15435666..15436116hg38UCSC Ensembl
chr9:15435664..15436114hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38451
hg19451
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280210
Samples
Known GenesSNAPC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571654
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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