A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559466



Internal ID20932537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:109139717..109147264hg38UCSC Ensembl
chr7:108779774..108787321hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg387548
hg197548
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273626
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559466
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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