A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17464405



Internal ID22522291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124016585..124023077hg38UCSC Ensembl
chr11:123887292..123893784hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg386493
hg196493
Variant TypeOTHER copy number variation
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5853910
Supporting Variants
Samples
Known GenesOR10G9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17464405
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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