A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17471721



Internal ID22529613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58179066..58189424hg38UCSC Ensembl
chr15:58471265..58481623hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3810359
hg1910359
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851080
Supporting Variants
Samples
Known GenesAQP9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17471721
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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