A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571772



Internal ID20944843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128158123..128158936hg38UCSC Ensembl
chr9:130920402..130921215hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38814
hg19814
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279969
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571772
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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