A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272594



Internal ID20839634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135191632..135192104hg38UCSC Ensembl
chr7:134876384..134876856hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38473
hg19473
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564374
Supporting Variants
Samples
Known GenesWDR91
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272594
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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