A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17466471



Internal ID22524363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:41972203..41982259hg38UCSC Ensembl
chr11:41993753..42003809hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3810057
hg1910057
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5854499
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17466471
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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