A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566826



Internal ID20939897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:100123664..100124132hg38UCSC Ensembl
chr7:99721287..99721755hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38469
hg19469
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272858
Samples
Known GenesCNPY4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566826
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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