A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217224



Internal ID20784264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16191754..16196307hg38UCSC Ensembl
chr10:16233753..16238306hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg384554
hg194554
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592472
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217224
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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