A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893719



Internal ID22668783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:142509473..142611090hg38UCSC Ensembl
chr4:143430626..143532243hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38101618
hg19101618
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415995
Samples
Known GenesINPP4B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893719
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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