A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227341



Internal ID20794381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28729985..28730753hg38UCSC Ensembl
chr10:29018914..29019682hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38769
hg19769
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579271
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227341
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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