A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5607118



Internal ID21555423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:138824720..138824720hg38UCSC Ensembl
chr4:139745874..139745874hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17133857
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5607118
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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