A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109150



Internal ID22018383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:88757023..88814571hg38UCSC Ensembl
chr11:88490191..88547739hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3857549
hg1957549
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578005
Samples
Known GenesGRM5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109150
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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