A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562290



Internal ID20935361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137434304..137436073hg38UCSC Ensembl
chr7:137119050..137120819hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg381770
hg191770
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272636
Samples
Known GenesDGKI
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562290
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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