A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17472989



Internal ID22530881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62184096..62192482hg38UCSC Ensembl
chr15:62476295..62484681hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg388387
hg198387
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5853901
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17472989
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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