A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591681



Internal ID20964752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46515203..46515963hg38UCSC Ensembl
chr11:46536753..46537513hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38761
hg19761
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227086
Samples
Known GenesAMBRA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591681
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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