A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575665



Internal ID20948736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18343841..18350934hg38UCSC Ensembl
chr11:18365388..18372481hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg387094
hg197094
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221408
Samples
Known GenesGTF2H1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575665
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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