A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17460809



Internal ID22518692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:39087594..39089219hg38UCSC Ensembl
chr11:39109144..39110769hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg381626
hg191626
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851332
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17460809
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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