A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227553



Internal ID20794593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26601029..26928130hg38UCSC Ensembl
chr10:26889958..27217059hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38327102
hg19327102
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586475
Supporting Variants
Samples
Known GenesABI1, LINC00202-2, PDSS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227553
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0001


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