A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5623480



Internal ID21571785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26484866..26484866hg38UCSC Ensembl
chr4:26486488..26486488hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38283
hg19283
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17136716
SamplesHG00512
Known GenesCCKAR
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5623480
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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