A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217589



Internal ID20784629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:36869930..36870784hg38UCSC Ensembl
chr10:37158858..37159712hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38855
hg19855
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583375
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217589
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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