A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226414



Internal ID20793454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117134523..117210043hg38UCSC Ensembl
chr11:117005239..117080759hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3875521
hg1975521
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6594810
Supporting Variants
Samples
Known GenesLOC100652768, PAFAH1B2, PCSK7, SIDT2, TAGLN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226414
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.41653


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