A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570656



Internal ID20943727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:115364775..115365527hg38UCSC Ensembl
chr9:118127054..118127806hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38753
hg19753
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279670
Samples
Known GenesDEC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570656
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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