A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595572



Internal ID20968643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62743222..62744504hg38UCSC Ensembl
chr11:62510694..62511976hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg381283
hg191283
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226984
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595572
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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