A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592985



Internal ID20966056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18246623..18268265hg38UCSC Ensembl
chr11:18268170..18289812hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3821643
hg1921643
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv979n223
Supporting Variantsnssv18223516
Samples
Known GenesSAA1, SAA2, SAA2-SAA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592985
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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