A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5586876



Internal ID21535432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:116244362..116244431hg38UCSC Ensembl
chr10:118003874..118003943hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17067538
SamplesNA19983
Known GenesGFRA1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5586876
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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