A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5608498



Internal ID21556803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:100448822..100448822hg38UCSC Ensembl
chr4:101369979..101369979hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17127668
SamplesHG00512
Known GenesEMCN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5608498
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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