A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595500



Internal ID20968571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67359472..67360225hg38UCSC Ensembl
chr11:67126943..67127696hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38754
hg19754
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221550
Samples
Known GenesLOC100130987
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595500
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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