A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219701



Internal ID20786741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74131679..74132373hg38UCSC Ensembl
chr11:73842724..73843418hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38695
hg19695
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593667
Supporting Variants
Samples
Known GenesC2CD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219701
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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