A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17468473



Internal ID22526362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15021136..15022135hg38UCSC Ensembl
chr11:15042682..15043681hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855888
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17468473
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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