A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555964



Internal ID20929035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132284877..132285613hg38UCSC Ensembl
chr9:135160264..135161000hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38737
hg19737
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280087
Samples
Known GenesSETX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555964
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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