A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583815



Internal ID20956886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68925118..68925997hg38UCSC Ensembl
chr10:70684874..70685753hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38880
hg19880
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv797n223
Supporting Variantsnssv18225158
Samples
Known GenesDDX50
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583815
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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