A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15704852



Internal ID21377128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44112328..44112541hg38UCSC Ensembl
chr10:44607776..44607989hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38214
hg19214
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4389354
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15704852
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0344828


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