A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592998



Internal ID20966069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47826585..47827271hg38UCSC Ensembl
chr11:47848137..47848823hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38687
hg19687
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225880
Samples
Known GenesNUP160
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592998
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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