A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558844



Internal ID20931915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130081399..130082740hg38UCSC Ensembl
chr9:132843678..132845019hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg381342
hg191342
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280040
Samples
Known GenesGPR107
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558844
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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