A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576676



Internal ID20949747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108523161..108523605hg38UCSC Ensembl
chr11:108393888..108394332hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38445
hg19445
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221797
Samples
Known GenesEXPH5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576676
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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