A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17567351



Internal ID21759394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:63982028..64066140hg38UCSC Ensembl
chr7:63442406..63526518hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3884113
hg1984113
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6109072
Supporting Variants
Samples
Known GenesLINC01005, ZNF727
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17567351
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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