A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269374



Internal ID20836414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151263619..151264649hg38UCSC Ensembl
chr6:151584754..151585784hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381031
hg191031
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6573706
Supporting Variants
Samples
Known GenesAKAP12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269374
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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