A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577703



Internal ID20950774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68908424..68908613hg38UCSC Ensembl
chr10:70668180..70668369hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38190
hg19190
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232711
Samples
Known GenesDDX50
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577703
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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