A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586038



Internal ID20959109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76953404..76954004hg38UCSC Ensembl
chr11:76664448..76665048hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227480
Samples
Known GenesACER3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586038
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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