A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221199



Internal ID20788239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:95750661..95751220hg38UCSC Ensembl
chr13:96402915..96403474hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38560
hg19560
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583006
Supporting Variants
Samples
Known GenesDNAJC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221199
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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