A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585507



Internal ID20958578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119177203..119177629hg38UCSC Ensembl
chr11:119047912..119048338hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38427
hg19427
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233275
Samples
Known GenesNLRX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585507
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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