A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568219



Internal ID20941290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:101584484..101585112hg38UCSC Ensembl
chr7:101227764..101228392hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38629
hg19629
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272908
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568219
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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