A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588958



Internal ID20962029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4033706..4034197hg38UCSC Ensembl
chr11:4054936..4055427hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38492
hg19492
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232258
Samples
Known GenesSTIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588958
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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