A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5636767



Internal ID21585072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:176644488..176644488hg38UCSC Ensembl
chr5:176071489..176071489hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38498
hg19498
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17125649
SamplesHG02492
Known GenesEIF4E1B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5636767
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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