A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545860



Internal ID20919084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16116174..16142632hg38UCSC Ensembl
chr1:16442669..16469127hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3826459
hg1926459
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247344
Samples
Known GenesEPHA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545860
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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