A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591315



Internal ID20964386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47575232..47576194hg38UCSC Ensembl
chr11:47596784..47597746hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38963
hg19963
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233031
Samples
Known GenesKBTBD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591315
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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