A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569381



Internal ID20942452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99481530..99482866hg38UCSC Ensembl
chr7:99079153..99080489hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg381337
hg191337
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275854
Samples
Known GenesZNF789
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569381
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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