A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591071



Internal ID20964142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78142090..78142582hg38UCSC Ensembl
chr11:77853136..77853628hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38493
hg19493
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222570
Samples
Known GenesKCTD21-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591071
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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