A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586671



Internal ID20959742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77704118..77704794hg38UCSC Ensembl
chr11:77415163..77415839hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38677
hg19677
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232140
Samples
Known GenesRSF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586671
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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