A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576261



Internal ID20949332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64956266..64956978hg38UCSC Ensembl
chr11:64723738..64724450hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38713
hg19713
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233975
Samples
Known GenesC11orf85
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576261
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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