A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271848



Internal ID20838888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:130230547..130231345hg38UCSC Ensembl
chr6:130551692..130552490hg19UCSC Ensembl
Cytoband6q23.1
Allele length
AssemblyAllele length
hg38799
hg19799
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571316
Supporting Variants
Samples
Known GenesSAMD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271848
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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