A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5608602



Internal ID21556907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26537086..26537086hg38UCSC Ensembl
chr4:26538708..26538708hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38410
hg19410
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17136104
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5608602
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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