A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18270743



Internal ID20837783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37215571..37216092hg38UCSC Ensembl
chr6:37183347..37183868hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38522
hg19522
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6572534
Supporting Variants
Samples
Known GenesTMEM217
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18270743
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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