A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17560989



Internal ID21885344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:54234014..54324272hg38UCSC Ensembl
chr7:54301707..54391965hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3890259
hg1990259
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6102698
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17560989
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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