A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15704861



Internal ID21377137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49900227..49900293hg38UCSC Ensembl
chr10:51108273..51108339hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4389362
Supporting Variants
Samples
Known GenesPARG
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15704861
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0517241


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