A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5616179



Internal ID21564484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:214887041..214887041hg38UCSC Ensembl
chr1:215060384..215060384hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg381671
hg191671
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17062654
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5616179
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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