A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576812



Internal ID20949883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122905716..122906370hg38UCSC Ensembl
chr11:122776424..122777078hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38655
hg19655
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236662
Samples
Known GenesC11orf63
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576812
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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