A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577797



Internal ID20950868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118577021..118577428hg38UCSC Ensembl
chr11:118447736..118448143hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38408
hg19408
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225441
Samples
Known GenesARCN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577797
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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