A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17471756



Internal ID22529648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68254024..68256967hg38UCSC Ensembl
chr15:68546362..68549305hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg382944
hg192944
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5866364
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17471756
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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