A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591393



Internal ID20964464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:104540974..104676112hg38UCSC Ensembl
chr10:106300732..106435870hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38135139
hg19135139
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv881n223
Supporting Variantsnssv18235927
Samples
Known GenesSORCS3, SORCS3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591393
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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