A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274091



Internal ID20841131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:7346927..7356869hg38UCSC Ensembl
chr6:7347160..7357102hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg389943
hg199943
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6560227
Supporting Variants
Samples
Known GenesCAGE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18274091
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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