A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577700



Internal ID20950771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67155636..67156256hg38UCSC Ensembl
chr11:66923107..66923727hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38621
hg19621
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222012
Samples
Known GenesKDM2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577700
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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