A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17365084



Internal ID22590753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:38349317..38350333hg38UCSC Ensembl
chr10:38638245..38639261hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg381017
hg191017
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5908688
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17365084
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.015


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