A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17472956



Internal ID22530848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59780424..59786812hg38UCSC Ensembl
chr15:60072623..60079011hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg386389
hg196389
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5861647
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17472956
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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