A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5635395



Internal ID21583700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:170278469..170278469hg38UCSC Ensembl
chr5:169705473..169705473hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17135789
SamplesNA19239
Known GenesLCP2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5635395
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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