A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560790



Internal ID20933861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:106794237..106806684hg38UCSC Ensembl
chr7:106434683..106447130hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3812448
hg1912448
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273569
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560790
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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