A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7953n223



Internal ID22810921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132912961..132914546hg38UCSC Ensembl
chr9:135788348..135789933hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg381586
hg191586
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6563688, nsv6556247
Samples
Known GenesTSC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7953n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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