A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5948198



Internal ID22723686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39329127..39329127hg38UCSC Ensembl
chr4:39330747..39330747hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412537
Samples
Known GenesMIR1273H, RFC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5948198
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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