A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5602513



Internal ID21551171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102676516..102677034hg38UCSC Ensembl
chr14:103142853..103143371hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38519
hg19519
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17086784
SamplesHG03125
Known GenesRCOR1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5602513
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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