A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588046



Internal ID20961117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76397989..76398540hg38UCSC Ensembl
chr11:76109033..76109584hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38552
hg19552
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1231n223
Supporting Variantsnssv18231131
Samples
Known GenesLOC100506127
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588046
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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