A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237982



Internal ID20805022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:37059682..37060214hg38UCSC Ensembl
chr15:37351883..37352415hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38533
hg19533
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581876
Supporting Variants
Samples
Known GenesMEIS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237982
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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