A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271371



Internal ID20838411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:44213135..44213660hg38UCSC Ensembl
chr6:44180872..44181397hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38526
hg19526
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571276
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271371
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00021


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