A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5569809



Internal ID21518171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:112957781..112957860hg38UCSC Ensembl
chr4:113878937..113879016hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17128901
SamplesHG03371
Known GenesANK2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5569809
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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