A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5597903



Internal ID21546524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14912807..14912980hg38UCSC Ensembl
chr10:14954806..14954979hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17069212
SamplesNA24385
Known GenesDCLRE1C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5597903
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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