A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591524



Internal ID20964595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:88865350..88866795hg38UCSC Ensembl
chr11:88598518..88599963hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg381446
hg191446
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217317
Samples
Known GenesGRM5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591524
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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