A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5608687



Internal ID21556992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39348470..39348470hg38UCSC Ensembl
chr4:39350090..39350090hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg383689
hg193689
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17131755
SamplesHG02492
Known GenesMIR1273H, RFC1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5608687
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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