A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17450636



Internal ID22508508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59384128..59404449hg38UCSC Ensembl
chr11:59151601..59171922hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3820322
hg1920322
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5865130
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17450636
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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