A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237968



Internal ID20805008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36443088..36443737hg38UCSC Ensembl
chr15:36735289..36735938hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38650
hg19650
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581301
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237968
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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