A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272255



Internal ID20839295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:116893262..116894190hg38UCSC Ensembl
chr7:116533316..116534244hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg38929
hg19929
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565517
Supporting Variants
Samples
Known GenesCAPZA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272255
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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