A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18270972



Internal ID20838012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:56675614..56676357hg38UCSC Ensembl
chr6:56540412..56541155hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38744
hg19744
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6569862
Supporting Variants
Samples
Known GenesDST, RNU6-71P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18270972
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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