A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17469544



Internal ID22527434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65685329..65690872hg38UCSC Ensembl
chr11:65452800..65458343hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg385544
hg195544
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855774
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17469544
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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