A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5602726



Internal ID21551385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13713817..13713875hg38UCSC Ensembl
chr10:13755817..13755875hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17069455
SamplesHG01505
Known GenesFRMD4A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5602726
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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