A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17365991



Internal ID22591660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:9295452..9295528hg38UCSC Ensembl
chr10:9337415..9337491hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5924450
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17365991
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.013


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