A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18280655



Internal ID20847695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36659919..36660995hg38UCSC Ensembl
chr9:36659916..36660992hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg381077
hg191077
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563431
Supporting Variants
Samples
Known GenesMELK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18280655
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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