A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17457269



Internal ID22515150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78437358..78438457hg38UCSC Ensembl
chr11:78148404..78149503hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5850576
Supporting Variants
Samples
Known GenesNARS2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17457269
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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