A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5635377



Internal ID21583682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168491947..168491947hg38UCSC Ensembl
chr4:169413098..169413098hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg386065
hg196065
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124499
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5635377
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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