A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17472937



Internal ID22530829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58140906..58151850hg38UCSC Ensembl
chr15:58433105..58444049hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3810945
hg1910945
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5866478
Supporting Variants
Samples
Known GenesAQP9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17472937
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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