A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5637407



Internal ID21585712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:170916060..170916060hg38UCSC Ensembl
chr5:170343064..170343064hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17131880
SamplesHG00731
Known GenesRANBP17
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5637407
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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