A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229798



Internal ID20796839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:104540873..104676090hg38UCSC Ensembl
chr10:106300631..106435848hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38135218
hg19135218
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581839
Supporting Variants
Samples
Known GenesSORCS3, SORCS3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229798
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00066


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