A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17457029



Internal ID22514910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15508235..15515045hg38UCSC Ensembl
chr11:15529781..15536591hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg386811
hg196811
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5856705
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17457029
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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