A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5616730



Internal ID21565035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37037065..37037065hg38UCSC Ensembl
chr4:37038687..37038687hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38186
hg19186
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17125318
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5616730
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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