A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5623738



Internal ID21572043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:112907587..112907587hg38UCSC Ensembl
chr2:113665164..113665164hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg381242
hg191242
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17107546
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5623738
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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