A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5578199



Internal ID21526663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:21104690..21108744hg38UCSC Ensembl
chr4:21106313..21110367hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg384055
hg194055
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17136319
SamplesNA19239
Known GenesKCNIP4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5578199
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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