A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272729



Internal ID20839769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23695416..23696550hg38UCSC Ensembl
chr7:23735035..23736169hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg381135
hg191135
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6572400
Supporting Variants
Samples
Known GenesFAM221A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272729
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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