A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5620107



Internal ID21568412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155064357..155064357hg38UCSC Ensembl
chr1:155036833..155036833hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38497
hg19497
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17060973
SamplesHG03009
Known GenesEFNA4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5620107
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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