A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566641



Internal ID20939712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110466586..110467644hg38UCSC Ensembl
chr9:113228866..113229924hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg381059
hg191059
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7910n223
Supporting Variantsnssv18279523
Samples
Known GenesSVEP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566641
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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