A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268614



Internal ID20835654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11916472..11917662hg38UCSC Ensembl
chr6:11916705..11917895hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg381191
hg191191
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571617
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268614
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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