A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274265



Internal ID20841305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66022659..66023309hg38UCSC Ensembl
chr7:65487646..65488296hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38651
hg19651
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566449
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18274265
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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