A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567228



Internal ID20940299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23278218..23279010hg38UCSC Ensembl
chr7:23317837..23318629hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38793
hg19793
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272686
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567228
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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