A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272332



Internal ID20839372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:121915679..121920633hg38UCSC Ensembl
chr7:121555733..121560687hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg384955
hg194955
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562075
Supporting Variants
Samples
Known GenesPTPRZ1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272332
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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