A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560600



Internal ID20933671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103321251..103323215hg38UCSC Ensembl
chr7:102961698..102963662hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg381965
hg191965
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272186
Samples
Known GenesDNAJC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560600
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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