A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576609



Internal ID20949680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61650636..61651553hg38UCSC Ensembl
chr11:61418108..61419025hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38918
hg19918
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226582
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576609
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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