A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272363



Internal ID20839403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:123686484..123751010hg38UCSC Ensembl
chr7:123326538..123391064hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3864527
hg1964527
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6558484
Supporting Variants
Samples
Known GenesWASL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272363
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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