A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583006



Internal ID20956077
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 StatusM
Merged Variants
Supporting Variantsnssv18221199
Samples
Known GenesDNAJC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583006
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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