A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274414



Internal ID20841454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139288725..139289707hg38UCSC Ensembl
chr7:138973471..138974453hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38983
hg19983
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570496
Supporting Variants
Samples
Known GenesUBN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18274414
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0002


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